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Etude chimique et spectroscopique du système B(SCH3)3-B(NCS)3
Reaction of trimethylthioborate, B(SMe) 3 , with triisothiocyanatoborane, B(NCS) 3 , at room temperature gives mixtures containing B(SMe) 3 , the mixed compounds B(NCS)(SMe) 2 and B(NCS) 2 (SMe) in low concentration, and association compounds. The previous compounds cannot be isolated due to equilib...
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Published in: | Canadian journal of chemistry 1979-05, Vol.57 (10), p.1122-1126 |
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Main Authors: | , , , |
Format: | Article |
Language: | eng ; fre |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Reaction of trimethylthioborate, B(SMe)
3
, with triisothiocyanatoborane, B(NCS)
3
, at room temperature gives mixtures containing B(SMe)
3
, the mixed compounds B(NCS)(SMe)
2
and B(NCS)
2
(SMe) in low concentration, and association compounds. The previous compounds cannot be isolated due to equilibria being set up. Mass spectrometry, infrared and nmr data are reported. Structures involving S-B donor-acceptor bonds between the monomers are proposed for the association compounds {B(NCS)
2
(SMe)}
2
, {B(NCS)
2
(SMe)}
2
{B(NCS)
3
}, and {B(NCS)
2
(SMe)}
2
{B(NCS)
3
}
2
. Reaction of these compounds with trimethylamine yields Me
3
NB(NCS)
3
and Me
3
NB(NCS)
2
(SMe). The same reaction with dimethylsulphide is incomplete and yields only Me
2
SB(NCS)
3
. Acidity strength decreases in the order B(NCS)
3
> B(NCS)
2
(SMe) > B(NCS)(SMe)
2
> B(SMe)
3
. This trend explains why dimerization of B(NCS)
2
(SMe) occurs whereas B(NCS)(SMe)
2
is unassociated. |
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ISSN: | 0008-4042 1480-3291 |
DOI: | 10.1139/v79-184 |