Synthesis of alkyl and aryl derivatives of closo-B12H122- by the palladium-catalyzed coupling of closo-B12H11I2- with Grignard reagents

被引:73
作者
Peymann, T [1 ]
Knobler, CB [1 ]
Hawthorne, MF [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
关键词
D O I
10.1021/ic9712075
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of [N(n-C4H9)(4)](2)[closo-B12H11I], [N(n-Bu)(4)](2)[2], with Grignard reagents, RMgX, in the presence of catalytic amounts of trans-Pd(PPh3)(2)Cl-2 and CuI in either tetrahydrofuran or 1,4-dioxane solution produced the corresponding alkylated or arylated polyhedral borane anions, closo-B12H11R2-, in good yield. By this method, we have synthesized [N(n-C4H9)(4)](2)[closo-B12H11CH3], [N(n-Bu)(4)](2)[3]; [N(n-C4H9)(4)](2)[closo-B12P11C6H5], [N(n-Bu)(4)](2)[4]; and Cs-2[closo-B12H11(n-C18H37)], Cs-2[5]. The structures of Cs-2[3] and PPN2[4] have been determined by X-ray diffraction studies. Crystallographic data are as follows: for Cs-2[3], orthorhombic, space group Pmcn, a = 954.6(6) pm, b = 1077.0(7) pm, c = 1396.8(9) pm, Z = 4, R = 0.055; for PPN2[3], which cocrystallized with two molecules of DMSO and one molecule of toluene, triclinic, space group P (1) over bar, a = 1138.4(10) pm, b = 1920.1(17) pm, c = 2143.2(18) pm, alpha = 93.26(2)degrees, beta = 104.43(2)degrees, gamma = 105.86(2)degrees, Z = 2, R = 0.076.
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页码:1544 / 1548
页数:5
相关论文
共 21 条
[1]   NA3[B20H17NH3] - SYNTHESIS AND LIPOSOMAL DELIVERY TO MURINE TUMORS [J].
FEAKES, DA ;
SHELLY, K ;
KNOBLER, CB ;
HAWTHORNE, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :3029-3033
[2]   SYNTHESIS OF S-ALKYL AND S-ACYL DERIVATIVES OF MERCAPTOUNDECAHYDRODODECABORATE, A POSSIBLE BORON CARRIER FOR NEUTRON-CAPTURE THERAPY [J].
GABEL, D ;
MOLLER, D ;
HARFST, S ;
ROSLER, J ;
KETZ, H .
INORGANIC CHEMISTRY, 1993, 32 (11) :2276-2278
[3]   PREPARATION AND CRYSTAL-STRUCTURES OF DIPYRIDINIOMETHANE MONOHALOGENOHYDRO-CLOSO-DODECABORATES(2-), [(C5H5N)(2)CH2][B(12)H(11)X] X=CL,BR,I [J].
HAECKEL, O ;
PREETZ, W .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1995, 621 (09) :1454-1458
[4]   IONIC ORGANOBORANES .4. PREPARATION AND PROPERTIES OF C7H6B10H9- AND C7H6B12H11- HEMIOUSENIDE IONS [J].
HARMON, KM ;
HARMON, AB ;
MACDONAL.AA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1969, 91 (02) :323-&
[5]   THE ROLE OF CHEMISTRY IN THE DEVELOPMENT OF BORON NEUTRON-CAPTURE THERAPY OF CANCER [J].
HAWTHORNE, MF .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1993, 32 (07) :950-984
[6]  
HAWTHORNE MF, 1997, J NEURO-ONCOL, V33, P55
[7]   Palladium-catalyzed coupling of ethynylated p-carborane derivatives: Synthesis and structural characterization of modular ethynylated p-carborane molecules [J].
Jiang, W ;
Harwell, DE ;
Mortimer, MD ;
Knobler, CB ;
Hawthorne, MF .
INORGANIC CHEMISTRY, 1996, 35 (15) :4355-4359
[8]   IODINATION REACTIONS OF ICOSAHEDRAL PARA-CARBORANE AND THE SYNTHESIS OF CARBORANE DERIVATIVES WITH BORON-CARBON BONDS [J].
JIANG, W ;
KNOBLER, CB ;
CURTIS, CE ;
MORTIMER, MD ;
HAWTHORNE, MF .
INORGANIC CHEMISTRY, 1995, 34 (13) :3491-3498
[9]   CHEMISTRY OF BORANES .30. CARBONYL DERIVATIVES OF B10H102- AND B12H122- [J].
KNOTH, WH ;
SAUER, JC ;
BALTHIS, JH ;
MILLER, HC ;
MUETTERTIES, EL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (19) :4842-+
[10]   CHEMISTRY OF BORANES .9. HALOGENATION OF B10H10-2 + B12H12-2 [J].
KNOTH, WH ;
MUETTERTIES, EL ;
MILLER, HC ;
CHIA, YT ;
SAUER, JC ;
BALTHIS, JH .
INORGANIC CHEMISTRY, 1964, 3 (02) :159-&