4.5 Article

Di-n-butyltin(IV)-catalyzed dimethyl carbonate synthesis from carbon dioxide and methanol: An in situ high pressure 119Sn{1H} NMR spectroscopic study

期刊

JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 696, 期 9, 页码 1904-1909

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2011.02.010

关键词

Diorganotin(IV); Carbon dioxide; Carbon dioxide utilization; Organic carbonates; High-pressure NMR spectroscopy; Catalysis

资金

  1. Centre National de la Recherche Scientifique
  2. Swiss National Foundation
  3. Schweitzerische Akademie der Technischen Wissenschaften [2009-12]
  4. French Ministry of Foreign Affairs [19148]

向作者/读者索取更多资源

The reactivity of five di-n-butyltin(IV) complexes, n-Bu2Sn(OR)(2) (1), n-Bu2SnO (3), [n-Bu2Sn(OR)](2)O (4), (n-Bu2SnO)(2)(CO2) (6) and (n-Bu2SnO)(6)[(n-Bu2SnOR)(2)(CO3)](2) (7) (R = CH3), with CO2, suggested as possible catalyst precursors and key-intermediates for the direct synthesis of dimethyl carbonate from carbon dioxide and methanol, has been investigated using high-pressure Sn-119{H-1} NMR (HP-NMR) spectroscopy. Four of the five precursors studied, i.e. 3, 4, 6 and 7 give rise to an identical Sn-119{H-1} NMR pattern which can be explicitly attributed to the fingerprint of the dimeric form of the 1-methoxy-3-methylcarbonatotetrabutyldistannoxane {5}(2). However, with 1, a new pair of signals is observed in addition to the characteristic Sn-119{H-1} NMR resonances of the dimeric hemicarbonato species {2}(2) and {5}(2), which can be attributed to the in situ formation of an unprecedented species suggested to be the trinuclear carbonato di-n-butyltin(IV) complex, 8. (C) 2011 Elsevier B. V. All rights reserved.

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