<?xml version="1.0" encoding="utf-8"?>
<articles xmlns:xlink="http://www.w3.org/1999/xlink">
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
An unusually large kinetic Br/Cl leaving group effect for the solvolysis of
1-halospiro[adamantane-2,2′-adamantane]
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a607628i</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kevill</surname>
<given-names>Dennis N.</given-names></name>
<name><surname>D’Souza</surname>
<given-names>Malcolm J.</given-names></name>
<name><surname>Lomas</surname>
<given-names>John S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>131</fpage>
<lpage>132</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a607628i">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a607628i">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Spin adduct formation from the spontaneous reaction between spin traps and
weak electron acceptors, as exemplified by trichloroacetonitrile. An acid
promoted version of the Forrester–Hepburn addition–oxidation
mechanism
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606864b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eberson</surname>
<given-names>Lennart</given-names></name>
<name><surname>MacCullough</surname>
<given-names>John J.</given-names></name>
<name><surname>Persson</surname>
<given-names>Ola</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>133</fpage>
<lpage>134</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606864b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606864b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Oxygen activation by metal complexes and alkyl hydroperoxides. Applications
of mechanistic probes to explore the role of alkoxyl radicals in alkane
functionalization
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606160e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>MacFaul</surname>
<given-names>Philip A.</given-names></name>
<name><surname>Arends</surname>
<given-names>Isabella W. C. E.</given-names></name>
<name><surname>Ingold</surname>
<given-names>Keith U.</given-names></name>
<name><surname>Wayner</surname>
<given-names>Danial D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>135</fpage>
<lpage>146</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606160e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606160e">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The synthesis of singlet ground state derivatives of non-Kekulé
polynuclear aromatics
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606932k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allinson</surname>
<given-names>Graeme</given-names></name>
<name><surname>Bushby</surname>
<given-names>Richard J.</given-names></name>
<name><surname>Jesudason</surname>
<given-names>Malini V.</given-names></name>
<name><surname>Paillaud</surname>
<given-names>Jean-Louis</given-names></name>
<name><surname>Taylor</surname>
<given-names>Norman</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>147</fpage>
<lpage>156</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606932k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606932k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;13&lt;/sup&gt;C NMR spectra of some unsymmetric
N,N′-dipyridyl ureas: spectral assignments and
molecular conformation
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606800f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Singha</surname>
<given-names>Netai C.</given-names></name>
<name><surname>Sathyanarayana</surname>
<given-names>Dixit N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>157</fpage>
<lpage>162</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606800f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606800f">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The synthesis, X-ray and solid state NMR studies of
2-N,N-diisopropylamino-1,3,2λ&lt;sup&gt;5&lt;/sup&gt;-
oxaselenaphospholane-2-selone
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606593g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Potrzebowski</surname>
<given-names>Marek J.</given-names></name>
<name><surname>BŁaszczyk</surname>
<given-names>Jarosław</given-names></name>
<name><surname>Wieczorek</surname>
<given-names>Michał W.</given-names></name>
<name><surname>Misiura</surname>
<given-names>Konrad</given-names></name>
<name><surname>Stec</surname>
<given-names>Wojciech J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>163</fpage>
<lpage>168</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606593g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606593g">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Rate constants and activation parameters for ring–chain tautomerism
in 5-, 6- and 7-ring-1,3-dinitrogen heterocycles
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606540f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Moodie</surname>
<given-names>Roy B.</given-names></name>
<name><surname>Moustras</surname>
<given-names>Marios Z.</given-names></name>
<name><surname>Read</surname>
<given-names>Gordon</given-names></name>
<name><surname>Sandall</surname>
<given-names>John P. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>169</fpage>
<lpage>172</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606540f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606540f">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Formation of thioketenes by thermal fragmentation of 1,2-dithiol-3-ones
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606411f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jørgensen</surname>
<given-names>Tonny</given-names></name>
<name><surname>Pedersen</surname>
<given-names>Carl Th.</given-names></name>
<name><surname>Flammang</surname>
<given-names>Robert</given-names></name>
<name><surname>Wentrup</surname>
<given-names>Curt</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>173</fpage>
<lpage>178</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606411f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606411f">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Effective charge development in the transfer of the acetyl group between
nucleophiles in acetonitrile solution: acetolysis and butylaminolysis of
substituted phenyl esters
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606402g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maude</surname>
<given-names>Antony B.</given-names></name>
<name><surname>Williams</surname>
<given-names>Andrew</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>179</fpage>
<lpage>184</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606402g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606402g">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
A novel host molecule
p-[1-(4-hydroxyphenyl)-1-methylethyl]calix[8]arene. Synthesis and
complexation properties in non-aqueous polar solution
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606270i</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tung</surname>
<given-names>Chen-Ho</given-names></name>
<name><surname>Ji</surname>
<given-names>Hai-Feng</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>185</fpage>
<lpage>188</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606270i">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606270i">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The effects of sulfur substitution in chiral amino thiols on the
enantioselective addition of organozinc reagents to aldehydes: a novel
method for estimation of free energies of dimerization in
monomer–dimer equilibria
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606133h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kang</surname>
<given-names>Jahyo</given-names></name>
<name><surname>Kim</surname>
<given-names>Jin Bum</given-names></name>
<name><surname>Kim</surname>
<given-names>Jeong Whan</given-names></name>
<name><surname>Lee</surname>
<given-names>Duckhwan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>189</fpage>
<lpage>194</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606133h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606133h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Formation and EPR spectra of radical species derived from the
oxidation of
the spin trap, α-phenyl-N-tert-butylnitrone
(PBN),
and some of its derivatives in 1,1,1,3,3,3-hexafluoropropan-2-ol.
Formation
of isoxazolidine radical cations
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606004h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eberson</surname>
<given-names>Lennart</given-names></name>
<name><surname>Hartshorn</surname>
<given-names>Michael P.</given-names></name>
<name><surname>Persson</surname>
<given-names>Ola</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>195</fpage>
<lpage>202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606004h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606004h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Proton chemical shifts in NMR. Part 8.&lt;sup&gt;1&lt;/sup&gt; Electric field effects
and fluorine substituent chemical shifts (SCS)
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a606003j</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>Raymond J.</given-names></name>
<name><surname>Warne</surname>
<given-names>Mark A.</given-names></name>
<name><surname>Griffiths</surname>
<given-names>Lee</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>203</fpage>
<lpage>208</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a606003j">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a606003j">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The relationship between structure and reactivity in RA-42, a
designed
helix–loop–helix motif
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605908b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lundh</surname>
<given-names>Ann-Christin</given-names></name>
<name><surname>Broo</surname>
<given-names>Klas</given-names></name>
<name><surname>Baltzer</surname>
<given-names>Lars</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>209</fpage>
<lpage>212</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605908b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605908b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Stacking and mobility of cationic amphiphiles in the complex with
DNA and
DNA transfection activity of the complex
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605729b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Akao</surname>
<given-names>Tetsuyuki</given-names></name>
<name><surname>Ito</surname>
<given-names>Akio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>213</fpage>
<lpage>218</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605729b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605729b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Intramolecular catalysis. Part 9.1 The hydrolysis of
p-nitrophenyl acetate catalysed by imidazoles having proximate
carboxylate groups
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605649k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>Keith</given-names></name>
<name><surname>Brownhill</surname>
<given-names>Andrew</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>219</fpage>
<lpage>222</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605649k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605649k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Calix[4]arene dimers; self-assembly via hydrogen bonding at the
upper rim
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605586i</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Struck</surname>
<given-names>Oliver</given-names></name>
<name><surname>Verboom</surname>
<given-names>Willem</given-names></name>
<name><surname>Smeets</surname>
<given-names>Wilberth J. J.</given-names></name>
<name><surname>Spek</surname>
<given-names>Anthony L.</given-names></name>
<name><surname>Reinhoudt</surname>
<given-names>David N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>223</fpage>
<lpage>228</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605586i">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605586i">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Theoretical and electrochemical study of the mechanism of
anthraquinone-mediated one-electron reduction of oxygen: the involvement of
adducts of dioxygen species to anthraquinones
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605549d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jeziorek</surname>
<given-names>Danuta</given-names></name>
<name><surname>Ossowski</surname>
<given-names>Tadeusz</given-names></name>
<name><surname>Liwo</surname>
<given-names>Adam</given-names></name>
<name><surname>Dyl</surname>
<given-names>Dariusz</given-names></name>
<name><surname>Nowacka</surname>
<given-names>Małgorzata</given-names></name>
<name><surname>Woźnicki(Deceased)</surname>
<given-names>Wiesław</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>229</fpage>
<lpage>236</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605549d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605549d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Complexation with diol host compounds. Part 24. Kinetics
of desolvation of inclusion compounds of 2,7-substituted
2,2′-bis(9-hydroxy-9-fluorenyl)biphenyl hosts with acetone
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605502h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caira</surname>
<given-names>Mino R.</given-names></name>
<name><surname>Coetzee</surname>
<given-names>Anita</given-names></name>
<name><surname>Nassimbeni</surname>
<given-names>Luigi R.</given-names></name>
<name><surname>Weber</surname>
<given-names>Edwin</given-names></name>
<name><surname>Wierig</surname>
<given-names>Andreas</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>237</fpage>
<lpage>242</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605502h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605502h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Solute–solvent and solvent–solvent interactions in binary
solvent mixtures. Part 5. Preferential solvation of solvatochromic
indicators in mixtures of propan-2-ol with hexane, benzene, ethanol and
methanol
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605421h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ràfols</surname>
<given-names>Clara</given-names></name>
<name><surname>Rosés</surname>
<given-names>Martí</given-names></name>
<name><surname>Bosch</surname>
<given-names>Elisabeth</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>243</fpage>
<lpage>248</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605421h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605421h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Further studies of intramolecular motions in crystalline ammonium bromides
by CP/MAS NMR
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605342d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Riddell</surname>
<given-names>Frank G.</given-names></name>
<name><surname>Rogerson</surname>
<given-names>Martin</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>249</fpage>
<lpage>256</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605342d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605342d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Application of the aromatic ring parameter (I ) to
solvolyses of β-arylalkyl toluene-p-sulfonates
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605340h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kevill</surname>
<given-names>Dennis N.</given-names></name>
<name><surname>D’Souza</surname>
<given-names>Malcolm J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>257</fpage>
<lpage>264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605340h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605340h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Azacyanocarbon chemistry. Comparison of the
hexacyano-3,4-diazahexa-1,5-dienediide
[C&lt;sub&gt;10&lt;/sub&gt;N&lt;sub&gt;8&lt;/sub&gt;]&lt;sup&gt;2−&lt;/sup&gt; with the corresponding
radical anion
[C&lt;sub&gt;10&lt;/sub&gt;N&lt;sub&gt;8&lt;/sub&gt;]˙&lt;sup&gt;−&lt;/sup&gt;:
electrochemical and EPR studies, crystallographic and electronic
structures
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a605243f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Decoster</surname>
<given-names>Marc</given-names></name>
<name><surname>Conan</surname>
<given-names>Françoise</given-names></name>
<name><surname>Kubicki</surname>
<given-names>Marek</given-names></name>
<name><surname>Mest</surname>
<given-names>Yves Le</given-names></name>
<name><surname>Richard</surname>
<given-names>Philippe</given-names></name>
<name><surname>Pala</surname>
<given-names>Jean Sala</given-names></name>
<name><surname>Toupet</surname>
<given-names>Loïc</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>265</fpage>
<lpage>272</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a605243f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a605243f">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Formation and X-ray structural study of enantiopure fused
1,5-oxathiocane derivatives
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604910i</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aversa</surname>
<given-names>Maria C.</given-names></name>
<name><surname>Barattucci</surname>
<given-names>Anna</given-names></name>
<name><surname>Bonaccorsi</surname>
<given-names>Paola</given-names></name>
<name><surname>Bruno</surname>
<given-names>Giuseppe</given-names></name>
<name><surname>Giannetto</surname>
<given-names>Placido</given-names></name>
<name><surname>Nicolò</surname>
<given-names>Francesco</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>273</fpage>
<lpage>278</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604910i">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604910i">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Electrostatic as well as hydrophobic interactions are important for the
association of Cpn60 (groEL) with peptides
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604880c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hutchinson</surname>
<given-names>Jonathan P.</given-names></name>
<name><surname>Oldham</surname>
<given-names>Timothy C.</given-names></name>
<name><surname>El-Thaher</surname>
<given-names>Talal S. H.</given-names></name>
<name><surname>Miller</surname>
<given-names>Andrew D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>279</fpage>
<lpage>288</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604880c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604880c">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Prediction of water–octanol partition coefficients using
theoretical descriptors derived from the molecular surface area and the
electrostatic potential
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604687h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haeberlein</surname>
<given-names>Markus</given-names></name>
<name><surname>Brinck</surname>
<given-names>Tore</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>289</fpage>
<lpage>294</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604687h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604687h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Hydrogen isotope fractionation factors for
N,N-dimethylbenzylammonium ion and some related
species: an unusually strong preference for deuterium over protium
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604674f</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Guo</surname>
<given-names>Hong-Xun</given-names></name>
<name><surname>Kresge</surname>
<given-names>A. Jerry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>295</fpage>
<lpage>298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604674f">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604674f">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Applicability and mathematical verification of the
reactivity–selectivity principle in the oxidation of thioanisoles
by oxo(salen)manganese(V) complexes 
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604602i</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chellamani</surname>
<given-names>Arunachalam</given-names></name>
<name><surname>Alhaji</surname>
<given-names>Naina Mohammed Ismail</given-names></name>
<name><surname>Rajagopal</surname>
<given-names>Seenivasan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>299</fpage>
<lpage>302</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604602i">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604602i">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Charge–transfer excitation of electron donor–acceptor
complexes of arylcyclopropanes
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604565k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Takahashi</surname>
<given-names>Yasutake</given-names></name>
<name><surname>Ohaku</surname>
<given-names>Hitoshi</given-names></name>
<name><surname>Nishioka</surname>
<given-names>Naoki</given-names></name>
<name><surname>Ikeda</surname>
<given-names>Hiroshi</given-names></name>
<name><surname>Miyashi</surname>
<given-names>Tsutomu</given-names></name>
<name><surname>Gormin</surname>
<given-names>David A.</given-names></name>
<name><surname>Hilinski</surname>
<given-names>Edwin F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>303</fpage>
<lpage>308</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604565k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604565k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Secondary steric effects in S&lt;sub&gt;N&lt;/sub&gt;Ar of thiophenes: a coordinate
kinetic, thermodynamic, UV–VIS, crystallographic and ab initio
study
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604516b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Consiglio</surname>
<given-names>Giovanni</given-names></name>
<name><surname>Frenna</surname>
<given-names>Vincenzo</given-names></name>
<name><surname>Mugnoli</surname>
<given-names>Angelo</given-names></name>
<name><surname>Noto</surname>
<given-names>Renato</given-names></name>
<name><surname>Pani</surname>
<given-names>Marcella</given-names></name>
<name><surname>Spinelli</surname>
<given-names>Domenico</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>309</fpage>
<lpage>316</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604516b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604516b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Visible-light induced photofixation of carbon dioxide into aromatic
ketones and benzyl halides catalysed by CdS
nanocrystallites 1
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604515d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fujiwara</surname>
<given-names>Hiroaki</given-names></name>
<name><surname>Kanemoto</surname>
<given-names>Masashi</given-names></name>
<name><surname>Ankyu</surname>
<given-names>Hirofumi</given-names></name>
<name><surname>Murakoshi</surname>
<given-names>Kei</given-names></name>
<name><surname>Wada</surname>
<given-names>Yuji</given-names></name>
<name><surname>Yanagida</surname>
<given-names>Shozo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>317</fpage>
<lpage>322</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604515d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604515d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The order of lithium ion affinities for the 20 common α-amino
acids. Calculation of energy-well depth of ion-bound
dimers
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604417d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andersen</surname>
<given-names>Ulla N.</given-names></name>
<name><surname>Bojesen</surname>
<given-names>Gustav</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>323</fpage>
<lpage>328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604417d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604417d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Acidity of dibasic carbon acids. Part 5.1–4 The
second acidity constant of
9,10-dihydrodibenz[a,h]anthracene in
tetrahydrofuran—geometry, charge distribution of dianion,
structure of dimetallic salts
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604331c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nir</surname>
<given-names>Malka</given-names></name>
<name><surname>Shapiro</surname>
<given-names>Israel O.</given-names></name>
<name><surname>Rabinovitz</surname>
<given-names>Mordecai</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>329</fpage>
<lpage>332</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604331c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604331c">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Effect of alkyl chain length on self-preorganization of artificial
nucleobase receptors
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604278c</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kuroda</surname>
<given-names>Yasuhisa</given-names></name>
<name><surname>Lintuluoto</surname>
<given-names>Juha M.</given-names></name>
<name><surname>Ogoshi</surname>
<given-names>Hisanobu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>333</fpage>
<lpage>340</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604278c">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604278c">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Acylphosphonate hemiketals—formation rate and equilibrium. The
electron-withdrawing effect of dimethoxyphosphinyl group
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604196e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katzhendler</surname>
<given-names>Jehoshua</given-names></name>
<name><surname>Ringel</surname>
<given-names>Israel</given-names></name>
<name><surname>Karaman</surname>
<given-names>Rafik</given-names></name>
<name><surname>Zaher</surname>
<given-names>Hisham</given-names></name>
<name><surname>Breuer</surname>
<given-names>Eli</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>341</fpage>
<lpage>350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604196e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604196e">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The thermal stability of S-nitrosothiols: experimental studies and
ab initio calculations on model compounds
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a604148e</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bainbrigge</surname>
<given-names>Nicola</given-names></name>
<name><surname>Butler</surname>
<given-names>Anthony R.</given-names></name>
<name><surname>Görbitz</surname>
<given-names>Carl</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>351</fpage>
<lpage>354</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a604148e">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a604148e">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Anthocyanin–aluminium and –gallium complexes in aqueous
solution
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a603851d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elhabiri</surname>
<given-names>M.</given-names></name>
<name><surname>Figueiredo</surname>
<given-names>P.</given-names></name>
<name><surname>Toki</surname>
<given-names>K.</given-names></name>
<name><surname>N</surname>
<given-names></given-names></name>
<name><surname>Saito</surname>
<given-names></given-names></name>
<name><surname>Brouillard</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>355</fpage>
<lpage>362</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a603851d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a603851d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Nuclear magnetic resonance investigations of calcium-antagonist
drugs. Part
4. Conformational and dynamic features of nicardipine {methyl
2-[methyl(phenylmethyl)amino]ethyl
1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
}
in deuterium oxide
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a603846h</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Calzolai</surname>
<given-names>Luigi</given-names></name>
<name><surname>Gaggelli</surname>
<given-names>Elena</given-names></name>
<name><surname>Maccotta</surname>
<given-names>Antonella</given-names></name>
<name><surname>Valensin</surname>
<given-names>Gianni</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>363</fpage>
<lpage>368</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a603846h">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a603846h">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Kinetic and equilibrium studies of σ-adduct formation and
nucleophilic substitution in the reactions of trinitro-activated benzenes
with aliphatic amines in acetonitrile
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a603707k</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crampton</surname>
<given-names>Michael R.</given-names></name>
<name><surname>Lord</surname>
<given-names>Simon D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>369</fpage>
<lpage>376</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a603707k">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a603707k">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Diastereoisomerism and electrochemical behaviour— an investigation
of redox-active cyclophanes
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a603333d</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Leitner</surname>
<given-names>Michael B.</given-names></name>
<name><surname>Kreher</surname>
<given-names>Thomas</given-names></name>
<name><surname>Sonnenschein</surname>
<given-names>Helmut</given-names></name>
<name><surname>Costisella</surname>
<given-names>Burkhard</given-names></name>
<name><surname>Springer</surname>
<given-names>Jürgen</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>377</fpage>
<lpage>382</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a603333d">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a603333d">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
Novel synthetic phospholipid protects lipid bilayers against oxidation
damage: role of hydration layer and bound water 
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a601955b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tirosh</surname>
<given-names>Oren</given-names></name>
<name><surname>Kohen</surname>
<given-names>Ron</given-names></name>
<name><surname>Katzhendler</surname>
<given-names>Jehoshua</given-names></name>
<name><surname>Gorodetsky</surname>
<given-names>Raphael</given-names></name>
<name><surname>Barenholz</surname>
<given-names>Yechezkel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>383</fpage>
<lpage>390</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a601955b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a601955b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society, Perkin Transactions 2</journal-title>
<issn>0300-9580</issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>
The expulsion of alkyl radicals from the methyliumylaminomethyl radical
cation, ˙CH&lt;sub&gt;2&lt;/sub&gt;NH&lt;sub&gt;2&lt;/sub&gt;CH&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;+&lt;/sup&gt;,
and related distonic ions
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/a601264g</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hammerum</surname>
<given-names>Steen</given-names></name>
<name><surname>Petersen</surname>
<given-names>Allan C.</given-names></name>
<name><surname>Sølling</surname>
<given-names>Theis I.</given-names></name>
<name><surname>Vulpius</surname>
<given-names>Tore</given-names></name>
<name><surname>Zappey</surname>
<given-names>Herman</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1997</year></pub-date>
<volume>1997</volume>
<issue>2</issue>
<fpage>391</fpage>
<lpage>396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=a601264g">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1997/P2/a601264g">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
</articles>
