Acyclic Telluroiminium Salts: Isolation and Characterization
摘要:
The isolation, structure, and reactions of acyclic telluroiminium salts were disclosed. The delocalization of electrons on the tellurium atom and the partial double-bond character of C-Te bonds in the salts are discussed on the basis of X-ray molecular structure analysis, 13C and 125Te NMR spectroscopy, and molecular orbital calculation.
Telluration of seleno- and chloroiminium salts leading to various telluroamides, and their structure and NMR properties
摘要:
The reaction of seleno- and chloroiminium salts with a tellurating agent derived from LiAlH4 and elemental tellurium gave telluro-amides in moderate to good yields. This new synthetic method enabled the isolation of the first aliphatic and secondary telluroamides. The molecular structure of an aromatic telluroamide was successfully revealed for the first time; the length of the C=Te bond in the aromatic telluroamide was the same as that in the telluroformamide-Cr complex, and the aromatic ring and Te=C-N moiety were not planar. Unlike the structure in the solid state, spectroscopic data of telluroamides suggest that there is conjugation between these two planes. The properties of the NMR spectra of a series of chalcogenoamides are also discussed. (c) 2006 Elsevier B.V. All rights reserved.
Telluration of seleno- and chloroiminium salts leading to various telluroamides, and their structure and NMR properties
作者:Yuichiro Mutoh、Toshiaki Murai、Shigeru Yamago
DOI:10.1016/j.jorganchem.2006.03.045
日期:2007.1
The reaction of seleno- and chloroiminium salts with a tellurating agent derived from LiAlH4 and elemental tellurium gave telluro-amides in moderate to good yields. This new synthetic method enabled the isolation of the first aliphatic and secondary telluroamides. The molecular structure of an aromatic telluroamide was successfully revealed for the first time; the length of the C=Te bond in the aromatic telluroamide was the same as that in the telluroformamide-Cr complex, and the aromatic ring and Te=C-N moiety were not planar. Unlike the structure in the solid state, spectroscopic data of telluroamides suggest that there is conjugation between these two planes. The properties of the NMR spectra of a series of chalcogenoamides are also discussed. (c) 2006 Elsevier B.V. All rights reserved.
Acyclic Telluroiminium Salts: Isolation and Characterization
作者:Yuichiro Mutoh、Toshiaki Murai、Shigeru Yamago
DOI:10.1021/ja044022n
日期:2004.12.1
The isolation, structure, and reactions of acyclic telluroiminium salts were disclosed. The delocalization of electrons on the tellurium atom and the partial double-bond character of C-Te bonds in the salts are discussed on the basis of X-ray molecular structure analysis, 13C and 125Te NMR spectroscopy, and molecular orbital calculation.