Synthesis and structural systematics of nitrogen base adducts of group 2 salts .1. Some adducts of group 2 halides with acetonitrile

被引:26
作者
Waters, AF
White, AH
机构
关键词
D O I
10.1071/CH9960027
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recrystallization of anhydrous Group 2 halides from anhydrous acetonitrile has yielded, in a number of cases, adducts MX(2).nMeCN suitable for characterization by room-temperature single-crystal X-ray studies, which revealed novel stereochemical types. Magnesium(II) bromide yields a trisolvate, ionic with disproportionated ligand arrays, as [Mg(NCMe)(6)] [MgBr4] (1), an unusual combination of homoleptic cationic and anionic species. Crystals are triclinic, PI, a 19.129(1), b 16.870(8), c 8.737(7) Angstrom, alpha 83.96(3), beta 87.93(4), gamma 65.24(2)degrees, Z = 4 f.u.; R was 0.068 for N-o 3181 'observed' (I > 3 sigma(1)) reflections. Mg-N are 2.12(2)-2.18(2) Angstrom, and Mg-Br are 2.452(7)-2.481(6) Angstrom. Calcium(II) bromide, by contrast, yields a disolvate; an infinite polymer, with the two MeCN ligands trans in a quasi-octahedral coordination sphere, and the polymer comprising a... Ca(mu-Br)(2)Ca(mu-Br)(2)... linear array. Crystals of 1:2 CaBr2/MeCN (2) are orthorhombic, Pbam, a 14.252(3), b 8.539(2), c 4.2088(9) Angstrom, Z = 2 f.u.; R 0.043 for N-o 352. Ca-N is 2.46(1) Angstrom, and Ca-Br 2.8765(9) Angstrom. CaI2 and SrI2 yield pentasolvates as neutral, molecular species [(MeCN)(5)MX(2)] (3) and (4), with the halides tra ns in a pentagonal bipyramidal coordination sphere. They are isomorphous, orthorhombic, Pcab, a approximate to 18.4, b approximate to 14.6, c approximate to 14.3 Angstrom, Z = 8 f.u.; R were 0.042 and 0.059 for N-o 2297 and 1489 respectively. Ca-I are 3.132(2), 3.116(2) Angstrom and Sr-I are 3.265(3), 3.238(3) Angstrom, while Ca-N are (range) 2.518(8)-2.566(8) Angstrom and Sr-N 2.68(2)-2.73(2) Angstrom.
引用
收藏
页码:27 / 34
页数:8
相关论文
共 24 条
[1]   THE CRYSTAL STRUCTURE OF CALCIUM BROMIDE [J].
BRACKETT, EB ;
BRACKETT, TE ;
SASS, RL .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1963, 25 (10) :1295-1296
[2]   SYNTHESIS AND CHARACTERIZATION OF [V(NCCH3)6-ZNCL4], A LOW VALENCE VANADIUM COMPLEX [J].
CHANDRASEKHAR, P ;
BIRD, PH .
INORGANICA CHIMICA ACTA-ARTICLES AND LETTERS, 1985, 97 (02) :L31-L33
[3]   STUDY OF CRYSTAL AND MOLECULAR-STRUCTURE OF BECL2(NCCH3)2 BY X-RAY-DIFFRACTION AND MO CALCULATIONS [J].
CHAVANT, C ;
DARAN, JC ;
JEANNIN, Y ;
KAUFMANN, G ;
MACCORDICK, J .
INORGANICA CHIMICA ACTA, 1975, 14 (03) :281-290
[4]   X-RAY CRYSTAL-STRUCTURE IDENTIFICATION OF THE TERNARY COMPLEX MGCL2.2SBCL3.6MECN [J].
DREW, MGB ;
CLAIRE, PPK ;
WILLEY, GR .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1988, (01) :215-218
[5]   Analysis of the complex-chemical behaviour of beryllium I [J].
Fricke, R ;
Ruschhaupt, F .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1925, 146 (1/2) :103-120
[6]   CRYSTAL AND MOLECULAR-STRUCTURES OF THE ANTIFERROMAGNETIC LINEAR-CHAIN HALIDE-BRIDGED COMPLEXES [CRX2(MECN)2](X = CL OR BR) [J].
HALEPOTO, DM ;
LARKWORTHY, LF ;
POVEY, DC ;
TUCKER, BJ ;
SMITH, GW .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1990, (02) :699-701
[7]  
HALL SR, 1992, EXTAL 3 2 REFERENCE
[8]  
HALL SR, 1992, XTAL USERS REFERENCE
[9]  
MACCORDICK J, 1974, CR ACAD SCI C CHIM, V278, P1177
[10]  
MACCORDICK J, 1975, B SOC CHIM FR I-PHYS, P107