Alkali metal compounds of a gallium(I) carbene analogue {:Ga[N(Ar)C(Me)]2} (Ar=2,6-iPr2C6H3)

被引:29
|
作者
Liu, Yanyan [1 ]
Li, Shaoguang [1 ]
Yang, Xiao-Juan [1 ]
Li, Qian-Shu [2 ]
Xie, Yaoming [3 ]
Schaefer, Henry F. [3 ]
Wu, Biao [1 ,4 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] S China Normal Univ, Sch Chem & Environm, Ctr Computat Quantum Chem, Guangzhou 510631, Guangdong, Peoples R China
[3] Univ Georgia, Ctr Computat Chem, Athens, GA 30602 USA
[4] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
基金
中国国家自然科学基金;
关键词
Gallium(I); NHCs analogue; Alkali metals; Ga-M bond; ALPHA-DIIMINE LIGANDS; ZINC-BONDED COMPOUND; STRUCTURAL-CHARACTERIZATION; COORDINATION CHEMISTRY; RING-SYSTEMS; MOLECULAR-STRUCTURE; GALLYL COMPLEXES; STABLE COMPOUND; REACTIVITY; HETEROCYCLES;
D O I
10.1016/j.jorganchem.2011.01.013
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A galliumdichloro complex (L center dot(-)) (GaCl2)-Cl-III (1) withan alpha-diimine ligand [(2,6-(Pr2C6H3)-Pr-i)NC(Me)](2) (L-0 represents the neutral ligand, L center dot- is the radical-anionic form of the ligand, and L represents its dianion L2-) was used to synthesize a series of alkali metal complexes of an N-heterocyclic carbenes (NHCs)-like gallium(I) species. Reduction of the precursor 1 with three equivalents of Na, Li, K or KC8, respectively, in THF gave the complexes [(LGaNa)-Na-I(THF)(3)] (2), [ (LGaLi)-Li-I(THF)(3)] (3), [LGaI{mu(2)-K(THF)(4)}(GaL)-L-I][K(THF)(6)] (4) and [LGaI(mu(2)-K){mu(2)-K(THF)(2)}(GaL)-L-I] (5). In these complexes, the original radical-anionic ligand was further reduced to the dianion, whereas the GaIII ion was reduced to Ga-I to yield the NHCs analogue [:GaN2C2](-), which then coordinated to alkali metal ions to form the complexes 2-5. Single crystal X-ray diffraction analyses revealed that these complexes feature direct Ga-M bonds (M=Li, Na, and K), which have also been studied by DFT computations. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1450 / 1455
页数:6
相关论文
共 50 条
  • [31] [HC{(CMe) (NAr)}2]Al[(NSiMe3)2N2] (Ar=2,6-iPr2C6H3):: The first five-membered AlN4 ring system
    Cui, CM
    Roesky, HW
    Schmidt, HG
    Noltemeyer, M
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2000, 39 (24) : 4531 - +
  • [32] Syntheses, structures and properties of [{HC(CMeNAr)2}Ge(E)X] (Ar=2,6-iPr2C6H3;: E = S, Se;: X = F, Cl)
    Ding, YQ
    Ma, QJ
    Roesky, HW
    Usón, I
    Noltemeyer, M
    Schmidt, HG
    DALTON TRANSACTIONS, 2003, (06) : 1094 - 1098
  • [33] Synthesis and characterization of the monomer Ga{(NDippCMe)2CH} (Dipp = C6H3Pri2-2,6):: a low valent gallium(I) carbene analogue
    Hardman, NJ
    Eichler, BE
    Power, PP
    CHEMICAL COMMUNICATIONS, 2000, (20) : 1991 - 1992
  • [34] The first structurally characterized aluminum compound with two SH groups:: [LAI(SH)2] (L=N(Ar)C(Me)CHC(Me)N(Ar), Ar=2,6-i-Pr2C6H3) and the catalytic properties of the sulfur P(NMe2)3 system
    Jancik, V
    Peng, Y
    Roesky, HW
    Li, JY
    Neculai, D
    Neculai, AM
    Herbst-Irmer, R
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (06) : 1452 - 1453
  • [35] A comparative study of π-arene-bridged lanthanum arylamide and aryloxide dimers.: Solution behavior, exchange mechanisms, and X-ray crystal structures of La2(NH-2,6-iPr2C6H3)6, La(NH-2,6-iPr2C6H3)3(THF)3, and La(NH-2,6-iPr2C6H3)3(py)2
    Giesbrecht, GR
    Gordon, JC
    Clark, DL
    Hay, PJ
    Scott, BL
    Tait, CD
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (20) : 6387 - 6401
  • [36] Tethered Heavy Dicarbene Analogues: Synthesis and Structure of Ditetryldiyl Ethers (Ar′E)2(μ-O) (E = Ge, Sn;Ar′ = C6H3-2,6-(C6H3-2,6-iPr2)2)
    Summerscales, Owen T.
    Olmstead, Marilyn M.
    Power, Philip P.
    ORGANOMETALLICS, 2011, 30 (13) : 3468 - 3471
  • [37] [{HC(CMeNAr)2}2Al2P4] (Ar=2,6-iPr2C6H3):: A reduction to a formal {P4},4- charged species
    Peng, Y
    Fan, HJ
    Zhu, HP
    Roesky, HW
    Magull, J
    Hughes, CE
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (26) : 3443 - 3445
  • [38] The first example of a μ2-imido functionality bound to a lanthanide metal center:: X-ray crystal structure and DFT study of [(μ-ArN)Sm(μ-NHAr)(μ-Me)AlMe2]2 (Ar = 2,6-iPr2C6H3)
    Gordon, JC
    Giesbrecht, GR
    Clark, DL
    Hay, PJ
    Keogh, DW
    Poli, R
    Scott, BL
    Watkin, JG
    ORGANOMETALLICS, 2002, 21 (22) : 4726 - 4734
  • [39] Spin-State Crossover with Structural Changes in a Cobalt(II) Organometallic Species: Low-Coordinate, First Row, Heteroleptic Amido Transition Metal Aryls. Synthesis and Characterization of Ar′MN(H)Ar# (M = Mn, Fe, Co) (Ar′ = C6H3-2,6-(C6H3-2,6-iPr2)2, Ar# = C6H3-2,6-(C6H2-2,4,6-Me3)2)
    Ni, Chengbao
    Fettinger, James C.
    Long, Gary J.
    Power, Philip P.
    INORGANIC CHEMISTRY, 2009, 48 (06) : 2443 - 2448
  • [40] Homologous series of heavier element dipnictenes 2,6-Ar2H3C6E=EC6H3-2,6-Ar2 (E = P, As, Sb, Bi; Ar=Mes=C6H2-2,4,6-Me3; or Trip = C6H2-2,4,6-iPr3) stabilized by m-terphenyl ligands
    Twamley, B
    Sofield, CD
    Olmstead, MM
    Power, PP
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (14) : 3357 - 3367