N,N′-dialkylimidazolium chloroplatinate(II), chloroplatinate(IV), and chloroiridate(IV) salts and an N-heterocyclic carbene complex of platinum(II):: Synthesis in ionic liquids and crystal structures

被引:92
作者
Hasan, M [1 ]
Kozhevnikov, IV [1 ]
Siddiqui, MRH [1 ]
Femoni, C [1 ]
Steiner, A [1 ]
Winterton, N [1 ]
机构
[1] Univ Liverpool, Leverhulme Ctr Innovat Catalysis, Dept Chem, Liverpool L69 7ZD, Merseyside, England
关键词
D O I
10.1021/ic000606o
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The first imidazole-type carbene complex of platinum(II), cis-(C2H4)(1-ethyl-3-methylimidazol-2-ylidene)PtCl2, has been obtained by reacting PtCl2 and PtC4 with ethylene in the basic [EMIM]Cl/AlCl3 (1.3:1) ionic liquid (where [EMIM](+) = 1-ethyl-3-methylimidazolium) at 200 degreesC and structurally characterized (monoclinic P2(1)/c space group, a = 10.416(2) Angstrom, b = 7.3421(9) Angstrom, c = 15.613(2) Angstrom, beta = 101.53(2)degrees, Z = 4). This complex can be regarded as a stable analogue of the pi -alkene-Pd(II)-carbene intermediate in the Heck reaction. In addition, a series of new N,N-dialkylimidazolium salts of platinum group metals of the type [RMIM](2)[MCln], where [RMIM+] = 1-alkyl-3-methylimidazolium and M = Pt(II), Pt(IV), or Ir(IV), have been prepared and characterized. The salts [EMIM](2)[PtCl6] (1) and [EMIM](2)[PtCl4] (2) were prepared in the ionic liquid [EMIM]Cl/AlCl3 and the salts [BMIM](2)[PtCl4] (3) and [BMIM](2)[PtCl6] (4) (where [BMIM](+) = 1-n-butyl-3-methylimidazolium) and [EMIM](2)[IrCl6] (5) in aqueous or acetonitrile media. From TGA measurements, salts 1-5 decompose in air in several steps eventually to form the corresponding metal, the onset of decomposition being observed at (degreesC) 260 (1), 220 (2), 200 (3), 215 (4),and 210 (5). The structures of 1, 2, and 5 were determined by single-crystal X-ray analysis. The three salts crystallize in the monoclinic P2(1)/n space group (1, a = 7.6433(9) Angstrom, b = 16.353(2) Angstrom, c 9.213(1) Angstrom, beta = 113.56(1)degrees, Z = 2; 2, a = 8.601(1) Angstrom, b = 8.095(2) Angstrom, c = 13.977(2) Angstrom, beta = 19.75(2)degrees, Z = 2; 5, a = 10.353(2) Angstrom, b = 9.759(2) Angstrom, c = 10.371(2) Angstrom, beta = 92.98(3)degrees, Z = 2).
引用
收藏
页码:795 / 800
页数:6
相关论文
共 51 条
  • [1] ROOM-TEMPERATURE IONIC LIQUIDS AS SOLVENTS FOR ELECTRONIC ABSORPTION-SPECTROSCOPY OF HALIDE-COMPLEXES
    APPLEBY, D
    HUSSEY, CL
    SEDDON, KR
    TURP, JE
    [J]. NATURE, 1986, 323 (6089) : 614 - 616
  • [2] Arduengo AJ, 1996, HETEROATOM CHEM, V7, P421, DOI 10.1002/(SICI)1098-1071(199611)7:6<421::AID-HC4>3.0.CO
  • [3] 2-B
  • [4] LOW-COORDINATE CARBENE COMPLEXES OF NICKEL(0) AND PLATINUM(0)
    ARDUENGO, AJ
    GAMPER, SF
    CALABRESE, JC
    DAVIDSON, F
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (10) : 4391 - 4394
  • [5] A STABLE CRYSTALLINE CARBENE
    ARDUENGO, AJ
    HARLOW, RL
    KLINE, M
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (01) : 361 - 363
  • [6] ELECTRONIC STABILIZATION OF NUCLEOPHILIC CARBENES
    ARDUENGO, AJ
    DIAS, HVR
    HARLOW, RL
    KLINE, M
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (14) : 5530 - 5534
  • [7] The heck reaction as a sharpening stone of palladium catalysis
    Beletskaya, IP
    Cheprakov, AV
    [J]. CHEMICAL REVIEWS, 2000, 100 (08) : 3009 - 3066
  • [8] Vanadium oxide complexes in room-temperature chloroaluminate molten salts
    Bell, RC
    Castleman, AW
    Thorn, DL
    [J]. INORGANIC CHEMISTRY, 1999, 38 (25) : 5709 - 5715
  • [9] Hydrophobic, highly conductive ambient-temperature molten salts
    Bonhote, P
    Dias, AP
    Papageorgiou, N
    Kalyanasundaram, K
    Gratzel, M
    [J]. INORGANIC CHEMISTRY, 1996, 35 (05) : 1168 - 1178
  • [10] FRIEDEL CRAFTS REACTIONS IN AMBIENT-TEMPERATURE MOLTEN-SALTS
    BOON, JA
    LEVISKY, JA
    PFLUG, JL
    WILKES, JS
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (04) : 480 - 483