Establishing coordination numbers for the lanthanides in simple complexes

被引:120
作者
Cotton, SA [1 ]
机构
[1] Uppingham Sch, Uppingham LE15 9QE, Rutland, England
关键词
lanthanide; complex; coordination number; agostic;
D O I
10.1016/j.crci.2004.07.002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This article reviews the development of the understanding of the coordination number in lanthanide complexes, showing how it was realized in the 1960s that lanthanide complexes frequently had much higher coordination numbers than 6, and how it subsequently became possible for chemists to synthesise compounds with coordination numbers as low as 2, 3 and 4. Subsequent sections examine how coordination of solvent can cause uncertainties in coordination numbers; the determination of the coordination number of the aqua ions and in hydrated salts; variations (or not) in coordination number across the lanthanide series; the effect of counter-ion upon coordination number; and agostic interactions and interactions with distant atoms (when is a bond not a bond?). To cite this article: S.A. Cotton, C. R. Chimie 8 (2004). (C) 2004 Academie des sciences. Published by Elsevier SAS. All rights reserved.
引用
收藏
页码:129 / 145
页数:17
相关论文
共 132 条
[1]  
AHRENS B, 2002, S J TEAT
[2]  
Ahrens B., UNPUB
[3]   GEOMETRY OF NONAAQUALANTHANOID(3+) COMPLEX IN SOLID BROMATES AND ETHYL SULFATES [J].
ALBERTSSON, J ;
ELDING, I .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1977, 33 (MAY13) :1460-1469
[4]   CRYSTAL AND MOLECULAR STRUCTURE OF TRINITRATOBIS (BIPYRIDYL)LANTHANUM(III) [J].
ALKARAGHOULI, AR ;
WOOD, JS .
INORGANIC CHEMISTRY, 1972, 11 (10) :2293-+
[5]   Coordination chemistry of trivalent lanthanide and actinide ions in dilute and concentrated chloride solutions [J].
Allen, PG ;
Bucher, JJ ;
Shuh, DK ;
Edelstein, NM ;
Craig, I .
INORGANIC CHEMISTRY, 2000, 39 (03) :595-601
[6]   Electronic structures of highly symmetrical compounds of f elements.: 37 [1] spectroscopic and structural characterization of Tris(2,6-di-t- butyl-phenolato)lanthanide(III) (Ln(OAr′)3; Ln = Pr, Nd), and parametric analysis of the crystal field splitting pattern of Nd(OAr′)3 [J].
Amberger, HD ;
Reddmann, H ;
Guttenberger, C ;
Unrecht, B ;
Zhang, LX ;
Apostolidis, C ;
Walter, O ;
Kanellakopulos, B .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 2003, 629 (09) :1522-1534
[7]  
Antsyshkina AS, 2002, RUSS J INORG CHEM+, V47, P361
[8]   Synthesis and structural characterisation of rare-earth bis(dimethylsilyl)amides and their surface organometallic chemistry on mesoporous MCM-41 [J].
Anwander, R ;
Runte, O ;
Eppinger, J ;
Gerstberger, G ;
Herdtweck, E ;
Spiegler, M .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1998, (05) :847-858
[9]   SYNTHESES, AND CRYSTAL AND MOLECULAR-STRUCTURES OF TETRAETHYLAMMONIUM [HEXAKIS(ISOTHIOCYANATO)LANTHANOIDATES(III)] INCLUDING AROMATIC HYDROCARBON OR HALOHYDROCARBON - [(C2H5)4N]3[M(NCS)6].G (M=ER, OR YB, G=BENZENE, FLUOROBENZENE, TOLUENE, OR CHLOROBENZENE) [J].
ARAI, H ;
SUZUKI, Y ;
MATSUMURA, N ;
TAKEUCHI, T ;
OUCHI, A .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1989, 62 (08) :2530-2535
[10]   SOME OXYGEN-DONOR COMPLEXES OF CYCLOPENTADIENYLURANIUM(IV) N-THIOCYANATE - STERIC CONSIDERATIONS AND STABILITY [J].
BAGNALL, KW ;
XINGFU, L .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1982, (07) :1365-1369