ELECTRON SPIN RESONANCE STUDIES OF THE STRUCTURE OF TRIARYLTIN RADICALS (ESR, ARYLTIN, SYNTHESIS).

Item

Title
ELECTRON SPIN RESONANCE STUDIES OF THE STRUCTURE OF TRIARYLTIN RADICALS (ESR, ARYLTIN, SYNTHESIS).
Identifier
AAI8614671
identifier
8614671
Creator
EL-HEFNAWI, SOBHY ABDEL HAMID.
Contributor
Fitzgerald B. Bramwell
Date
1986
Language
English
Publisher
City University of New York.
Subject
Chemistry, Physical
Abstract
Electron spin resonance (ESR) spectra of isotopically enriched (('119)Sn) triphenyltin, triparatolyltin and triorthotolyltin radicals in rigid glass solution are reported at 4 K and 93 K. Radicals were generated by visible light photo-oxidation of triaryltin anions. Anions were synthesized by alkali metal reduction of tetraryltin in 2-methyltetrahydrofuran.;The isotropic and anisotropic hyperfine splitting have been determined using the Breit-Rabi equation. From this data we have used a semi-empirical approach to estimate the "S" and "P" character of the orbital containing the unpaired electron, the extent of hybridization, the ligand-tin-ligand bond angle, (PHI), and the ligand-symmetry axis complementary angle, (THETA), (out-of-plane bond angle).;From an analysis of the spectra, the following conclusions were drawn: triphenyltin and triparatolyltin radicals appear to be relatively stable, pyramidal structures with ligand-tin-ligand bond angles of 114.6(DEGREES), and 114.8(DEGREES), respectively. Ligand-symmetry axis complementary angles are 1.36(DEGREES), 13.4(DEGREES), respectively.;Triorthotolyltin radical appears to have a deeper pyramidal structure with a ligand-tin-ligand bond angle of 114.4(DEGREES) and a ligand-symmetry axis complementary angle of 13.9(DEGREES). These results are discussed in terms of limited tin-carbon multiple bonding and in terms of steric effects.
Type
dissertation
Source
PQT Legacy CUNY.xlsx
degree
Ph.D.
Program
Chemistry
Item sets
CUNY Legacy ETDs