A BONDING REACTIVITY RELATIONSHIP FOR NI(PCY3)2(CO2) - A COMPARATIVE SOLID-STATE SOLUTION NUCLEAR-MAGNETIC-RESONANCE STUDY (P-31, C-13) AS A DIAGNOSTIC-TOOL TO DETERMINE THE MODE OF BONDING OF CO2 TO A METAL CENTER

被引:49
作者
ARESTA, M
GOBETTO, R
QUARANTA, E
TOMMASI, I
机构
[1] UNIV BARI, CNR, CTR MISO, I-70126 BARI, ITALY
[2] UNIV TURIN, DIPARTIMENTO CHIM INORGAN CHIM FIS & CHIM MAT, I-10125 TURIN, ITALY
关键词
D O I
10.1021/ic00047a015
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
P-31 and C-13 nuclear magnetic resonance spectra in the solid state and in solution, at variable temperature, have been used for the first time to determine a direct correlation of the modes of bonding Of CO2 in Ni(PCY3)2(CO2) in the two states. In solution, at 173 K, CO2 is eta2-CO bonded to nickel and P-31 and C-13 chemical shifts are almost identical with the value found for the solid complex, while a dynamic process averages, in solution, the two phosphorus atoms (DELTAG(double dagger) = 39.3 kJ mol-1) at room temperature through an intramolecular motion. The modification of the mode of bonding of CO2 to a metal center that occurs when a solid sample is dissolved in a solvent may be relevant to the reactivity of CO2-transition metal complexes, as shown by the reaction of coordinated CO2 with electrophiles (H+, Ag+) and H-2. The temperature can play an important role.
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页码:4286 / 4290
页数:5
相关论文
共 45 条
[31]   SYNTHESIS AND REACTIVITY OF A HETEROMETALLIC CO2 COMPLEX [J].
LUNDQUIST, EG ;
HUFFMAN, JC ;
FOLTING, K ;
MANN, BE ;
CAULTON, KG .
INORGANIC CHEMISTRY, 1990, 29 (01) :128-134
[32]   FORMATION OF A HETEROMETALLIC CARBON-DIOXIDE COMPLEX WITH CONCURRENT REDUCTION OF CO2 [J].
LUNDQUIST, EG ;
HUFFMAN, JC ;
CAULTON, KG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (26) :8309-8310
[33]   EVIDENCE FOR OXIDE TRANSFER FROM COORDINATED CO-2 TO COORDINATED CO IN AN ANIONIC CO-2 COMPLEX [J].
MAHER, JM ;
LEE, GR ;
COOPER, NJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (24) :6797-6799
[34]  
MASCETTI J, IN PRESS
[35]   REACTIVITY OF SOME TRANSITION-METAL SYSTEMS TOWARD LIQUID CARBON-DIOXIDE [J].
MASON, MG ;
IBERS, JA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (19) :5153-5157
[36]   A MOLECULAR-ORBITAL ANALYSIS OF THE BONDING CAPABILITIES OF CARBON-DISULFIDE AND CARBON-DIOXIDE TOWARD TRANSITION-METAL FRAGMENTS [J].
MEALLI, C ;
HOFFMANN, R ;
STOCKIS, A .
INORGANIC CHEMISTRY, 1984, 23 (01) :56-65
[37]   DETERMINATION OF P-31 CHEMICAL SHIELDING TENSORS FROM NMR-STUDIES ON SINGLE-CRYSTALS OF CHLOROTRIS(TRIPHENYLPHOSPHINE) RHODIUM(I) [J].
NAITO, A ;
SASTRY, DL ;
MCDOWELL, CA .
CHEMICAL PHYSICS LETTERS, 1985, 115 (01) :19-23
[38]   NET [2 + 2] CYCLOADDITION REACTIONS OF THE OXO COMPLEXES CP2M=O (M = MO, W) WITH ELECTROPHILIC ORGANIC AND ORGANOMETALLIC SUBSTRATES - FORMATION OF BIMETALLIC MU-2-ETA-3-CO2 COMPLEXES [J].
PILATO, RS ;
HOUSMEKERIDES, CE ;
JERNAKOFF, P ;
RUBIN, D ;
GEOFFROY, GL ;
RHEINGOLD, AL .
ORGANOMETALLICS, 1990, 9 (08) :2333-2341
[39]   NET [2 + 2] CYCLO-ADDITION OF THE METAL-OXO BONDS OF CP2M=O (CP = C5H5-M = MO, W) ACROSS THE CARBON-OXYGEN BOND OF CARBONYL LIGANDS TO FORM MU-2, ETA-3-CO2 COMPLEXES [J].
PILATO, RS ;
GEOFFROY, GL ;
RHEINGOLD, AL .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1989, (17) :1287-1288
[40]   FUNDAMENTAL-STUDIES ON P-31 RELAXATION MECHANISMS - THE IMPORTANCE OF CHEMICAL-SHIFT ANISOTROPY AND ITS IMPLICATIONS FOR P-31 NMR-STUDIES OF ORGANOMETALLIC COMPOUNDS [J].
RANDALL, LH ;
CARTY, AJ .
INORGANIC CHEMISTRY, 1989, 28 (06) :1194-1196