Issue 2, 1996

Time-resolved study of the transients produced in the CO2 and ArF laser flash photolysis of gaseous silacyclobutane and 1,3-disilacyclobutane

Abstract

A time-resolved study of the transients produced in the TEA CO2 or ArF laser-induced decomposition of gaseous silacyclobutane (SCB) and 1,3-disilacyclobutane (DSCB) is reported. Both compounds produce transient H2C[double bond, length as m-dash]SiH2 as the major primary product, which has been identified by its optical absorption spectrum, with λmax≈ 260 nm. Under conditions of low laser fluence, this species has two decay channels: a unimolecular process (k= 2.3 ± 0.7 × 104 s–1) and a reaction with the parent compound (kSCB= 2.0 ± 0.3 × 10–13 cm3 molecule–1 s–1 and kDSCB= 3.0 ± 0.5 × 10–13 cm3 molecule–1 s–1). At high fluence (7.2 J cm–2 for the CO2 laser and 6 J cm–2 for the ArF laser), the transient absorption signals become very complex owing to the onset of a number of other reactions and the formation of several additional transient species which appear to have strong absorption in the 250–650 nm region, with peaks/shoulders at ca. 260, 320 and 435 nm but these could not be identified unambiguously.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans., 1996,92, 179-183

Time-resolved study of the transients produced in the CO2 and ArF laser flash photolysis of gaseous silacyclobutane and 1,3-disilacyclobutane

S. Dhanya, A. Kumar, R. K. Vatsa, R. D. Saini, J. P. Mittal and J. Pola, J. Chem. Soc., Faraday Trans., 1996, 92, 179 DOI: 10.1039/FT9969200179

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements