Monoorganobismuth(III) dihalides containing the new pincer 2,6-{MeN(CH2CH2)2NCH2}2C6H3 ligand: solution NMR, vibrational and single-crystal X-ray studies

被引:32
作者
Soran, Albert [1 ]
Breunig, Hans J. [2 ]
Lippolis, Vito [3 ]
Arca, Massimiliano [3 ]
Silvestru, Cristian [1 ]
机构
[1] Univ Babes Bolyai, Fac Chim Ingn Chim, RO-400028 Cluj Napoca, Romania
[2] Univ Bremen, Inst Anorgan & Phys Chem, D-28334 Bremen, Germany
[3] Univ Cagliari, Dipartimento Chim Inorgan & Analit, I-09042 Monserrato, CA, Italy
关键词
SOLID-STATE STRUCTURE; SOLUTION BEHAVIOR; ORGANOBISMUTH COMPOUNDS; BISMUTH COMPOUNDS; INTRAMOLECULAR COORDINATION; DYNAMIC-BEHAVIOR; EDGE INVERSION; AB-INITIO; CHEMISTRY; 2-(ME2NCH2)C6H4;
D O I
10.1039/b811713f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of RLi [R = 2,6-{MeN(CH2CH2)(2)NCH2}(2)C6H3] with BiCl3 (1:1 molar ratio) afforded RBiCl2 (2). RBiBr2 (3) and RBiI2 (4) were obtained by halogen-exchange reactions from 2. The organobismuth(III) dihalides containing the new steric demanding (N, C, N)-pincer ligand were characterized both in solution and solid state. The molecular structures of compounds 2-4 were established by single-crystal X-ray diffraction. They all show a T-shaped CBiX2 core, stabilized by two strong intramolecular N -> Bi interactions in trans positions to each other. The overall (N, C, N)BiX2 core exhibits a distorted square-pyramidal coordination geometry. The NMR studies provided evidences for the presence of internal nitrogen-bismuth coordination in solution too. DFT calculations were performed on the related species [2,6-(R2NCH2)(2)C6H3]BiX2 (R = H, Me; X = Cl, Br, I) in order to elucidate the bond nature and vibrational spectroscopic features of these compounds.
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页码:77 / 84
页数:8
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