Issue 1, 1985

Tin-119 Mössbauer and nuclear magnetic resonance studies of organotin compounds. Part 1. Sterically crowded tetraorganotin derivatives

Abstract

119 Sn Mössbauer and 119Sn n.m.r. data are presented for a series of sterically hindered tetra-organotin derivatives. For adamant-1-yl (ad) derivatives two quadrupole splittings (q.s.) are observed and the values of the tin chemical shifts, δ(119Sn), are significantly more negative (resonances at higher field) than expected. Thus Sn(ad)4 shows the presence of q.s. with values of 2.70 and 0.76 mm s–1 at 80 K. These tin sites are discussed. The δ(119Sn) value of –73.5 p.p.m. (relative to SnMe4) indicates increased electron density at the tin atom probably resulting from charge separation of the type ad3[graphic omitted]. Other sterically hindered derivatives show similar features, although less dramatically. The additivity effect of tin substituents in this series is also discussed. Long relaxation times were recorded for the more sterically hindered derivatives. The Mössbauer spectrum at 80 K for quench-frozen SnPh4 is also presented. The spectrum shows a singlet with a large linewidth, which narrows on annealing at 193 K to give a very narrow line. The wide line is easily explained in terms of the known crystal structure.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1985, 169-175

Tin-119 Mössbauer and nuclear magnetic resonance studies of organotin compounds. Part 1. Sterically crowded tetraorganotin derivatives

C. S. Frampton, R. M. G. Roberts, J. Silver, J. F. Warmsley and B. Yavari, J. Chem. Soc., Dalton Trans., 1985, 169 DOI: 10.1039/DT9850000169

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