Photochemical synthesis of N-adamantylhomoallylamines through addition of cyclic olefins to imines catalyzed by alumina grafted cadmium sulfide
Photochemical synthesis of N-adamantylhomoallylamines through addition of cyclic olefins to imines catalyzed by alumina grafted cadmium sulfide
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DOI:
10.1039/c1pp05298e
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发表时间:
2012-01-01
影响因子:
3.1
通讯作者:
Kisch, Horst
中科院分区:
文献类型:
--
作者:
Aldemir, Muege;Heinemann, Frank W.;Kisch, Horst
Grafting cadmium sulfide onto alumina induces a small bandgap widening and a more significant lifetime variation of the light generated charge carriers from 0.76 microseconds measured for pristine CdS to 0.75, 0.86, and 1.20 microseconds found for CdS/Al2O3 containing 30, 20, and 9% of CdS, respectively. The quasi-Fermi level of electrons of -0.42 V (NHE) is not significantly changed. These alumina grafted semiconductor photocatalysts enable the linear addition of cyclopentene, cyclohexene, and alpha-pinene to N-adamantylimines affording novel homoallyladamantylamines in isolated yields of 21-85% through a regioselective C-C heterocoupling of intermediate allyl and alpha-aminobenzyl radicals. As by-products hydrodimers of the imine are formed by C-C homocoupling of the benzylic radicals. Different from heterocoupling, the homocoupling is a stereospecific process directed by the nature of the olefin employed in the reaction.