Thermal and Catalytic Dehydrogenation of the Guanidine-Borane Adducts H3B•hppH (hppH=1,3,4,6,7,8-hexahydro-2H-pyrimidol[1,2-a]pyrimidine) and H3B•N(H)C(NMe2)2: A Combined Experimental and Quantum Chemical Study

被引:25
|
作者
Ciobanu, Oxana [1 ]
Allouti, Faycal [1 ]
Roquette, Pascal [1 ]
Leingang, Simone [1 ]
Enders, Markus [1 ]
Wadepohl, Hubert [1 ]
Himmel, Hans-Joerg [1 ]
机构
[1] Univ Heidelberg, Inst Anorgan Chem, D-69120 Heidelberg, Germany
关键词
Dehydrogenation; Homogeneous catalysis; Heterogeneous catalysis; Hydrogen; Boron; Density functional calculations;
D O I
10.1002/ejic.200800564
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Herein thermal and catalytic dehydrogenation of the guanidine-borane adducts H3B center dot hppH (hppH = 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine) and H3B center dot N(H)C(NMe2)(2) are analysed. Thermal decomposition of H3B center dot hppH at 80 degrees C leads to [HB(mu-hpp)](2) and a second boron hydride, which is tentatively identified as [(kappa N-2-hpp)BH2]. Decomposition in boiling toluene (110 degrees C) leads to a mixture of [H2B(mu-hpp)](2) and [HB(mu-hpp)](2), from which [H2B(mu-hpp)](2) can be separated and crystallised. In the presence of a catalyst (with Cp2TiCl2/nBuLi or [Rh(1,5-cod)Cl](2) as precatalysts) dehydrogenation at 80 degrees C leads predominantly to [H2B(mu-hpp)](2). In the case of H3B center dot N(H)C(NMe2)(2) uncatalysed dehydrogenation turns out to be a very slow process even at 110 degrees C. Interestingly, the ultimate product of this process is oligomeric methylimino borane, [HBNMe](n). This pathway can be modelled and understood with the aid of quantum chemical calculations. Faster dehydrogenation can be initiated by addition of a catalyst. Finally, the possible mechanisms for thermal and CP2Ti-catalysed dehydrogenation are analysed for the model compound H3B center dot N(H)C(NH2)(2) by means of quantum chemical (DFT) calculations. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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页码:5482 / 5493
页数:12
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