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1.
K. H. Geib J. Reitstötter R. E. Liesegang Thomas M. Richter Thierbach P. Krais 《Colloid and polymer science》1938,84(1):119-122
Ohne Zusammenfassung 相似文献
2.
Keller Teichmann Hans Pfeiffer W. Langenbeck A. Reid Heinrich Menzel Th. Höpner W. Mühlsteph M. Ulmann Geib R. E. Liesegang 《Colloid and polymer science》1939,87(1):100-104
Ohne Zusammenfassung 相似文献
3.
A new class of dithiostannanes and dithiogermanes have been prepared from 1,1'-binaphthyl-2,2'-dithiol and 3,3'-bis(trimethylsilyl)-1,1'-binaphtho-2,2'-dithiol. While reduction of 4-butyl-4-chloro-3,5-dithia-4-stanna-cyclohepta[2,1-a;3,4-a']dinaphthalene to the corresponding tin hydride was unsuccessful, 4-tert-butyl-3,5-dithia-4-germa-cyclohepta[2,1-a;3,4-a']dinaphthalene and 4-tert-butyl-2,6-bis(trimethylsilyl)-3,5-dithia-4-germa-cyclohepta[2,1-a;3,4-a']dinaphthalene were obtained by reduction of the parent germanium chlorides with NaBH(4) and LiBH(4), respectively. Kinetic constants for hydrogen transfer to a primary alkyl radical were measured for both germanium hydrides. Reduction of alpha-halo carbonyl compounds by these germanium hydrides occurs with moderate ee values (up to 42%), while hydrogermylation of methyl methacrylate occurs with low selectivity (<3/1) for the former hydride but high selectivity (>10/1) for the latter. 相似文献
4.
Shao L Geib SJ Badger PD Cooper NJ 《Journal of the American Chemical Society》2002,124(50):14812-14813
We have established cation/anion coupling reactions between the tropylium ligand in [M(eta7-C7H7)(CO)3]+ (M = Cr, W) and the reductively activated eta4-benzene ligand in [Mn(eta4-C6H6)(CO)3]- (3-) to form [M(CO)3(mu2-eta6:eta5-C7H7-C6H6)Mn(CO)3]; [Cr(CO)3(mu2-eta6:eta5-C7H7-C6H6)Mn(CO)3] can be further reduced to [Cr(CO)3(mu2-eta5:eta4-C7H7-C6H6)Mn(CO)3]2-, in which the tropylium and benzene ligands have undergone a [2 + 2] cross coupling reaction. 相似文献
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John Fredericks Ji Yang Steven J. Geib Andrew D. Hamilton 《Journal of Chemical Sciences》1994,106(5):923-935
In this short review we describe approaches to the design and construction of synthetic molecules that mimic the process of
self organization that is at the heart of biological complexity. Multi-subunit enzymes, viruses, and higher order DNA structures
are formed by the non-covalent association of many smaller components. This self-assembly is controlled by the nature, number
and orientation of interacting groups on the surface of the subunits. The central problem lies in overcoming the unfavorable
entropy of multi-subunit association by significant enthalpic contribution from the binding of complementary regions on the
subunits. We will place particular emphasis on the design of synthetic molecules that use hydrogen bonding interactions to
control the formation of aggregates of well-defined structure. 相似文献