Volume 20, Issue 22
Organoelement Compounds
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ChemInform Abstract: The Rate of Ring Closure of 1,1-Dimethyl-2-phenyl-1-silabuta-1,3-diene to 1,1-Dimethyl-2-phenyl-1-silacyclobutene.

R. T. CONLIN

R. T. CONLIN

Dep. Chem., Univ. North Tex., Denton, TX 76203, USA

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S. ZHANG

S. ZHANG

Dep. Chem., Univ. North Tex., Denton, TX 76203, USA

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M. NAMAVARI

M. NAMAVARI

Dep. Chem., Univ. North Tex., Denton, TX 76203, USA

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K. L. BOBBITT

K. L. BOBBITT

Dep. Chem., Univ. North Tex., Denton, TX 76203, USA

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M. J. FINK

M. J. FINK

Dep. Chem., Univ. North Tex., Denton, TX 76203, USA

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First published: May 30, 1989

Abstract

Irradiation of (II) in a 3-methylpentane glass at 77 K yields the siladiene (I) whose UV spectrum displays a maximum wavelength at 338 nm.

ChemInform Abstract

Irradiation of (II) in a 3-methylpentane glass at 77 K yields the siladiene (I) whose UV spectrum displays a maximum wavelength at 338 nm. Flash photolysis of (II) produces the same reactive siladiene (I), which cyclizes to the starting ring structure. The barrier for the activation energy which is necessary for the ring closure reaction is given. The rate constant for this reaction is compared to that of polymerization. Trapping studies with Me3Si-O-Me support both the kinetic and spectral assignments.

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