Infrared spectroscopic characterization of cyanocuprates

被引:51
作者
Huang, H
Alvarez, K
Lui, Q
Barnhart, TM
Snyder, JP
PennerHahn, JE
机构
[1] EMORY UNIV, DEPT CHEM, ATLANTA, GA 30329 USA
[2] UNIV MICHIGAN, DEPT CHEM, WILLARD H DOW LABS, ANN ARBOR, MI 48109 USA
关键词
D O I
10.1021/ja961862w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthetically useful cyanocuprates MeCu(CN)Li (2) and ''Me(2)CuLi . LiCN'' (3) have been characterized by infrared spectroscopy. Titration of CuCN . 2LiCl (1) with MeLi in THF solution has established that 2 has an IR absorption due to cyanide stretching at 2133 cm(-1) with epsilon = 2.3 x 10(3) cm(-2) M(-1), while the CN stretching frequency for 3 occurs at 2115 cm(-1) with epsilon = 4.0 x 10(2) cm(-2) M(-1). The spectra suggest that 2 and 3 are the only significant cuprate species present in the methylcyanocuprate system. The IR titration data give a formation constant of approximately 8 x 10(3) for 2 + MeLi reversible arrow 3. The present data stand in contrast to earlier reports that 2 and 3 have identical IR spectra. The earlier conclusion appears to have been a consequence of the significantly different molar absorptivity of cyanide in 2 and 3 and the presence of small amount of 2 in equilibrium with 3 when the MeLi: CuCN ratio is 2:1, Ab initio calculations of the frequencies and intensities of the CN stretch are able to semiquantitatively reproduce the observed trends using a model in which the CN- is bound to the Cu in 2 but is not bound directly to the Cu in 3, The predicted CN stretch for a ''higher order'' cyanocuprate structure, with a three-coordinate [Me(2)CuCN](2-), is not consistent with the observed value. In contrast, the seven-membered bridged Gilman cuprate 14 appears to fulfill all of the structural and IR spectroscopic requirements for the 2115 cm(-1) species.
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页码:8808 / 8816
页数:9
相关论文
共 48 条
[1]   DENSITY FUNCTIONAL GAUSSIAN-TYPE-ORBITAL APPROACH TO MOLECULAR GEOMETRIES, VIBRATIONS, AND REACTION ENERGIES [J].
ANDZELM, J ;
WIMMER, E .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (02) :1280-1303
[2]   STRUCTURE AND BONDING OF THE TRANSITION-METAL METHYL AND PHENYL COMPOUNDS MCH(3) AND MC(6)H(5) (M=CU,AG,AU) AND M(CH3)(2) AND M(C6H5)(2) (M=ZN,CD,HG)(1) [J].
ANTES, I ;
FRENKING, G .
ORGANOMETALLICS, 1995, 14 (09) :4263-4268
[3]   STRUCTURAL CHARACTERIZATION OF ORGANOCOPPER COMPLEXES BY EXAFS AND XANES - EVIDENCE THAT CYANIDE DOES NOT COORDINATE TO CU IN DIMETHYL CUPRATE SOLUTIONS [J].
BARNHART, TM ;
HUI, H ;
PENNERHAHN, JE .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (14) :4310-4311
[4]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[5]   NEW COPPER CHEMISTRY .20. LITHIUM CYANOCUPRATES, RCU(CN)LI - 1ST OBSERVATION OF 2-BOND C-13-C-13 NMR COUPLINGS IN ORGANOCUPRATES [J].
BERTZ, SH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (14) :5470-5471
[6]   NEW COPPER CHEMISTRY .17. HIGHER-ORDER CYANOCUPRATES - ARE THEY REAL [J].
BERTZ, SH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (10) :4031-4032
[7]   It's on lithium! An answer to the recent communication which asked the question: 'If the cyano ligand is not on copper, then where is it?' [J].
Bertz, SH ;
Miao, GB ;
Eriksson, M .
CHEMICAL COMMUNICATIONS, 1996, (07) :815-816
[8]   FACTORS GOVERNING THE THERMAL-STABILITY OF ORGANOCOPPER REAGENTS - 2 NEW CLASSES OF HETEROCUPRATES WITH GREATLY IMPROVED THERMAL-STABILITY [J].
BERTZ, SH ;
DABBAGH, G .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1982, (18) :1030-1032
[9]   ELECTRONIC COUPLING IN CYANO-BRIDGED RUTHENIUM POLYPYRIDINE COMPLEXES AND ROLE OF ELECTRONIC EFFECTS ON CYANIDE STRETCHING FREQUENCIES [J].
BIGNOZZI, CA ;
ARGAZZI, R ;
SCHOONOVER, JR ;
GORDON, KC ;
DYER, RB ;
SCANDOLA, F .
INORGANIC CHEMISTRY, 1992, 31 (25) :5260-5267
[10]  
BOHME M, 1994, ORGANOMETALLICS, V13, P4237