SYNTHESIS, CHARACTERIZATION AND ELECTRONIC-STRUCTURE OF THE NOVEL STELLATED OCTAHEDRAL CLUSTER [CO-6(MU(3)-S)(7)(MU(3)-H)-(PET(3))(6)](+) - CRYSTAL AND MOLECULAR-STRUCTURE OF [CO-6(MU(3)-S)(7)-(MU(3)-H)(PET(3))(6)](0.7)[CO-6(MU(3)-S)(8)(PET(3))(6)](0.3)[BPH(4)]

被引:9
作者
CECCONI, F
GHILARDI, CA
MIDOLLINI, S
ORLANDINI, A
ZANELLO, P
CINQUANTINI, A
BENCINI, A
UYTTERHOEVEN, MG
GIORGI, G
机构
[1] UNIV SIENA,DIPARTIMENTO CHIM,I-53100 SIENA,ITALY
[2] UNIV FLORENCE,DIPARTIMENTO CHIM,I-50144 FLORENCE,ITALY
[3] UNIV SIENA,CTR INTERDIPARTIMENTALE ANAL & DETERMINAZ STRUTTU,I-53100 SIENA,ITALY
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1995年 / 23期
关键词
D O I
10.1039/dt9950003881
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reaction of Co(O(2)CMe)(2) . 4H(2)O with an excess of PEt(3) and H2S afforded the novel diamagnetic octahedral cluster [Co-6(mu(3)-S)(7)(mu(3)-H)(PEt(3))(6)](+) together with a minor amount of the known paramagnetic isostructural [Co-6(mu(3)-S)(8)(PEt(3))(6)](+). Solid solutions of the two cluster cations have been isolated as the BPh(4)(-) salt. The deuteriated derivative [Co-6(mu(3)-S)(7)(mu(3)-D)(PEt(3))(6)](+) has been prepared for comparison. The compounds have been characterized by H-1, P-31 NMR, mass spectrometry and electrochemical measurements. The molecular structure of a sample of composition [Co-6(mu(3)-S)(7)(mu(3)-H)(PEt(3))(6)](0.7)[Co-6(mu(3)-S)(8)(PEt(3))(6)](0.3)[BPh(4)] has been determined by single-crystal X-ray diffraction. It consists of a solid solution of [Co-6(mu(3)-S)(7)(mu(3)-H)(PEt(3))(6)](+) and [Co-6(mu(3)-S)(8)(PEt(3))(6)](+). The cation [Co-6(mu(3)-S)(7)(mu(3)-H)(PEt(3))(6)](0.7)[Co-6(mu(3)-S)(8)(PEt(3))(6)](+)(0.3) is isostructural with the series [M(6)(mu(3)-S)(8)(PEt(3))(6)](n+), having a metal-metal separation averaging 2.739(8) A. The electronic structure of the novel hydridoderivative has been investigated through density functional calculations.
引用
收藏
页码:3881 / 3889
页数:9
相关论文
共 41 条
[1]  
ADAMS R, 1994, ORGANOMETALLICS, V13, P2356
[2]  
AGRESTI A, 1984, INORG CHEM, V24, P689
[3]  
[Anonymous], 1974, INT TABLES XRAY CRYS, VIV, p[99, 149]
[4]   Self-consistent molecular Hartree-Fock-Slater calculations - I. The computational procedure [J].
Baerends, E. J. ;
Ellis, D. E. ;
Ros, P. .
CHEMICAL PHYSICS, 1973, 2 (01) :41-51
[5]  
Baerends E. J., 1992, J COMPUT PHYS, V99, P84, DOI DOI 10.1016/0021-9991(92)90277-6
[6]   CRYSTAL AND MOLECULAR-STRUCTURE, MAGNETIC-PROPERTIES AND SCATTERED-WAVE DESCRIPTION OF THE ELECTRONIC-STRUCTURE OF THE HEXANUCLEAR OCTAHEDRAL CLUSTERS [FE-6(MU(3)-S)(8)(PET(3))(6)][PF6](N) (N=1 OR 2) [J].
BENCINI, A ;
GHILARDI, CA ;
MIDOLLINI, S ;
ORLANDINI, A ;
RUSSO, U ;
UYTTERHOEVEN, MG ;
ZANCHINI, C .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1995, (06) :963-974
[7]   ELECTRONIC-STRUCTURE AND MAGNETIC-PROPERTIES OF THE HEXANUCLEAR OCTAHEDRAL CLUSTER [CO6(MU-3-S)8(PET3)6]BPH4 [J].
BENCINI, A ;
MIDOLLINI, S ;
ZANCHINI, C .
INORGANIC CHEMISTRY, 1992, 31 (11) :2132-2137
[8]   ELECTRONIC-STRUCTURE OF PARAMAGNETIC CLUSTERS OF TRANSITION-METAL IONS .3. MAGNETIC-PROPERTIES AND SCATTERED WAVE DESCRIPTION OF THE ELECTRONIC-STRUCTURE OF THE HEXANUCLEAR OCTAHEDRAL CLUSTER [FE6(MU-3-S)8(PET3)6](BPH4)2 [J].
BENCINI, A ;
UYTTERHOEVEN, MG ;
ZANCHINI, C .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 1994, 52 (04) :903-918
[9]  
BENCINI A, IN PRESS INORG CHIM
[10]   SITE-SELECTIVE SUBSTITUTION-REACTIONS AND ISOMERIZATIONS IN TETRAHEDRAL MCO3 CARBONYL CLUSTERS (M=FE, RU) AND N, P, S, AND TE DONOR LIGANDS - CRYSTAL-STRUCTURES OF HRUCO3(CO)10(PME2PH)2 AND HRUCO3(CO)9(PME2PH)3 [J].
BRAUNSTEIN, P ;
ROSE, J ;
TOUSSAINT, D ;
JAASKELAINEN, S ;
AHLGREN, M ;
PAKKANEN, TA ;
PURSIAINEN, J ;
TOUPET, L ;
GRANDJEAN, D .
ORGANOMETALLICS, 1994, 13 (06) :2472-2479