Reaction and crystal structures of 1,3-bis(trimethylsilyl)-2-t-butyl-aza-allyl-lithium with iron(II), cobalt(II), nickel(II), titanium(IV)

被引:0
作者
Zhang Yong [1 ]
Guo Jian-Ping [1 ]
Tong Hong-Bo [1 ]
Huang Shu-Ping [1 ]
Liu Dian-Sheng [1 ]
机构
[1] Shanxi Univ, Sch Chem & Chem Engn, Taiyuan 030006, Peoples R China
关键词
1,3-bis(trimethylsilyl)-2-tert-butyl-aza-allyl-lithium; 1,3-bis(trimethylsilyt)-2-tert-butyl-aza-allyl cobalt; coupling meso-compound; crystal structure;
D O I
暂无
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Aza-allyl lithium [LiN(R)C(Bu-t)CHR](2) (R = SiMe3) reacted with NiCl2 or TICl4 to produce a coupling meso-compound [N(SiMe3)C(Bu-t)CH(SiMe3)], (1), or with CoCl2, FeCl2 (mole ratio 2:1) to produce complex 1,3-bis (trimethylsilyl)-2-t-butyl-aza-allyl cobalt(II) (2) and 1,3-bis(trimethylsilyl)-2-t-butyl-aza-allyl iron(II) (3) respectively. Compounds 1, 2 and 3 were characterized by elemental analysis, H-1 and C-13 NMR spectra and X-ray single crystal diffraction. The results show that the compound 1 belongs to the triclinic space group P (1) over bar. A centro-symmetric dimer aggregation is observed with the two moiety positioned in trans manner. The complex 2 belongs to the monoclinic. space group C2/c. The molecular structure of 2 is rigorous centro-symmetry. The six coordination atoms of two 1-aza-allyl ligands organize the distorted octahedral field of central cobalt atom. The structure of 3 is similar to complex 2. CCDC: 219193, 1; 219194, 2; 219195, 3.
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页码:1175 / 1179
页数:5
相关论文
共 11 条
[1]  
ANDREWS PC, 1989, CHEM COMMUN, P1341
[2]   Alkali metal-1-azaallyl complexes: X-ray crystallographic, NMR spectroscopic and ab initio calculational studies [J].
Armstrong, DR ;
Clegg, W ;
Dunbar, L ;
Liddle, ST ;
MacGregor, M ;
Mulvey, RE ;
Reed, D ;
Quinn, SA .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1998, (20) :3431-3436
[3]  
AVENT AG, 2004, J ORGANOMET CHEM, V3, P2591
[4]  
CATHERINE E, 2001, INORG CHEM, P752
[5]  
CATHERINE FC, 2001, COORDIN CHEM REV, V219, P605
[6]   Synthesis and structures of crystalline lithium 1-azaallyls and a 1,3-diazaallyl derived from Li{CH(SiMe3)(SiMe3-n(OMe)n)}(n=1 or 2) and Li{CH(SiMe2OMe)2} and RCN (R = tBu, Ph, 2,5-Me2C6H3, or Ad) [J].
Hitchcock, PB ;
Lappert, MF ;
Wei, XH .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2003, 683 (01) :83-91
[7]   Synthesis, characterisation and reactions of 1,3-bis(trimethylsilyl)-1-aza-allyl-lanthanide complexes;: X-ray structures of [Sm(LL′)2I(thf)], [Yb(LL′)2] and [RN=C(But)CH(R)]2 (thf=tetrahydrofuran, LL′=η3-N(R)C(But)CHR, R=SiMe3) [J].
Hitchcock, PB ;
Lappert, MF ;
Tian, S .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1997, 549 (1-2) :1-12
[8]   Reactions of LiCHR2 and related lithium alkyls with α-H free nitriles and the crystal structures of eleven representative lithium 1,3-diazaallyls, 1-azaallyls and β-diketiminates [J].
Hitchcock, PB ;
Lappert, MF ;
Layh, M ;
Liu, DS ;
Sablong, R ;
Shun, T .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 2000, (14) :2301-2312
[9]  
HITCHCOCK PB, 1994, SOC CHEM COMMUN, P2637
[10]   RECENT STUDIES ON METAL AND METALLOID BIS(TRIMETHYLSILYL) METHYLS AND THE TRANSFORMATION OF THE BIS(TRIMETHYLSILYL) METHYL INTO THE AZAALLYL AND BETA-DIKETINIMATO LIGANDS [J].
LAPPERT, MF ;
LIU, DS .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1995, 500 (1-2) :203-217