BONDING ANALYSIS IN INORGANIC TRANSITION-METAL CUBIC CLUSTERS .2. METAL-CENTERED HEXACAPPED M(9)(MU(4)-E)(6)L(8) SPECIES

被引:23
作者
FURET, E [1 ]
LEBEUZE, A [1 ]
HALET, JF [1 ]
SAILLARD, JY [1 ]
机构
[1] UNIV RENNES 1,CHIM SOLIDE & INORGAN MOLEC LAB,CNRS,URA 1495,F-35042 RENNES,FRANCE
关键词
D O I
10.1021/ja00122a026
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The bonding in metal-centered M(9)(mu(4)-E)(6)L(8) cubic clusters is analyzed by means of extended Huckel and self-consistent field-multiple scattering-X alpha calculations. Different electron counts are allowed depending on the magnitude of the interaction of the interstitial metal atom (M(c)) with its metallic cubic host (M(s)) and the nature of the capping E ligands (either bare or substituted). In all cases, a strong interaction is observed between the s and p AOs of the encapsulated atom and metallic MOs of the cube. Significant additional M(c)-M(s) bonding is obtained if strong interactions occur between the five d AOs and corresponding metallic MOs. This still hypothetical situation, which leads to a count of 120 metallic valence electrons (MVEs). is favored for long M(s)-M(s) and short M(c)-E contacts. Another closed-shell configuration, corresponding to 124 MVEs, is obtained if the interaction of the M(c) t(2g) d AOs with the metallic cube is large and the e(g) one weak. This is the case for Ni-9(mu(4)-GeEt)(6)(CO)(8). Electron counts corresponding to open-shell ground-state configurations can occur when the capping E ligands are strong donors and/or when the MVE count is larger than 120. In such cases, the levels which may be partly populated an of e(g), t(2g), and (for large electron counts) t(1g) symmetry. For example, the ground-state electron distribution of the 124-MVE clusters Pd-9(mu(4)-E)(6)(PPh(3))(8) (E = As, Sb) corresponds to (t(2g))(4)(e(g))(0)(t(1g))(0), while it is found to be (e(g))(4)(t(1g))(4)(t(2g))(2) for the 150-MVE cluster Ni-9(mu(4)-Te)(6)(PEt(3))(8). The various possibilities for the electron distribution in these levels are discussed for various MVE counts, in relation to the M-M and M-E bond distances and the nature of E. The possibility of incorporating main-group elements at the center of the metallic cube is also discussed.
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页码:4936 / 4944
页数:9
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共 37 条
[1]   A SCALE OF ELECTRONEGATIVITY BASED ON ELECTROSTATIC FORCE [J].
ALLRED, AL ;
ROCHOW, EG .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1958, 5 (04) :264-268
[2]   ELECTRONEGATIVITIES OF CARBON, SILICON, GERMANIUM, TIN AND LEAD [J].
ALLRED, AL ;
ROCHOW, EG .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1958, 5 (04) :269-288
[3]   COUNTERINTUITIVE ORBITAL MIXING IN SEMI-EMPIRICAL AND ABINITIO MOLECULAR-ORBITAL CALCULATIONS [J].
AMMETER, JH ;
BURGI, HB ;
THIBEAULT, JC ;
HOFFMANN, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1978, 100 (12) :3686-3692
[4]   THE TRANSITION FROM MOLECULES TO SOLIDS - MOLECULAR SYNTHESES OF NI9TE6(PET3)8, NI20TE18(PET3)12, AND NITE [J].
BRENNAN, JG ;
SIEGRIST, T ;
STUCZYNSKI, SM ;
STEIGERWALD, ML .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (26) :9240-9241
[5]   NEW COPPER CLUSTERS CONTAINING SE AND PET3 AS LIGANDS - [CU70SE35(PET3)22] AND [CU20SE13(PET3)12] [J].
FENSKE, D ;
KRAUTSCHEID, H .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1990, 29 (12) :1452-1454
[6]   SYNTHESES AND CRYSTAL-STRUCTURES OF [PD9AS8(PPH3)8] AND [PD9SB6(PPH3)8] [J].
FENSKE, D ;
PERSAU, C .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1991, 593 (02) :61-68
[7]   PD CLUSTERS CONTAINING AS AND PPH3 LIGANDS - THE STRUCTURES OF [PD9AS6(PPH3)8], [PD2(AS2)(PPH3)4], AND [PD20AS12(PPH3)12] [J].
FENSKE, D ;
FLEISCHER, H ;
PERSAU, C .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1989, 28 (12) :1665-1667
[8]   [NI9(MU-4-AS)6(PPH3)5CL3], A CUBIC BODY-CENTERED NI9-CLUSTER [J].
FENSKE, D ;
MERZWEILER, K ;
OHMER, J .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1988, 27 (11) :1512-1513
[9]  
FENSKE D, IN PRESS Z ANORG ALL
[10]   BONDING ANALYSIS IN INORGANIC TRANSITION-METAL CUBIC CLUSTERS .1. NONCENTERED HEXACAPPED M8(MU-4-E)6LN (N-LESS-THAN-OR-EQUAL-TO-8) SPECIES [J].
FURET, E ;
LEBEUZE, A ;
HALET, JF ;
SAILLARD, JY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (01) :274-280