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排序方式: 共有139条查询结果,搜索用时 15 毫秒
1.
2.
William L. Jolly 《Journal of organometallic chemistry》1979,172(2):C33-C35
Substitution of the hydrogen atoms of the cyclopentadienyl ring of (N, N-dimethylaminomethyl)cymantrene by deuterium changes the direction of orientation of metalation of this amine. 相似文献
3.
P.W. Jolly C. Krüger R. Salz J.C. Sekutowski 《Journal of organometallic chemistry》1979,165(3):C39-C42
The stoichiometric reaction between allene, zerovalent nickel and a chelating diphosphane leads to the formation of a bis-methylenenickelacyclopentane derivative whose structure has been established by X-ray crystallography. 相似文献
4.
Bis ( η1, η2-allyl) palladium phosphine complexes react with carbon dioxide and sulphur dioxide by insertion into the palladium-carbon σ-bond to give η3-allylpalladium-carboxylate and -S-sulphinate complexes. 相似文献
5.
When core ionization of an atom in a molecule causes significant changes in bond orders, the core-hole ion is formed in a strained configuration. This strain causes vibrational broadening of the core line. The core-hole ion can be represented as an ordinary chemical species by applying the equivalent cores approximation. Then simple rules of classical valence bond theory can be used to predict changes in the weighting of resonance structures and corresponding changes in bond orders. Thus qualitative changes in relative linewidths can be predicted. 相似文献
6.
B. Henc P.W. Jolly R. Salz S. Stobbe G. Wilke R. Benn R. Mynott K. Seevogel R. Goddard C. Krüger 《Journal of organometallic chemistry》1980,191(2):449-475
A series of 1 : 1 adducts have been prepared by treating the bis-η3-allyl complexes of nickel, palladium and platinum with tertiary phosphines. Investigations of their structure in solution as well as in the crystal have shown that both 18-electron (η3-allyl)2ML complexes as well as 16-electron (η1-allyl)-(η3-allyl)ML complexes may be formed. 相似文献
7.
P. Jolly K. V. Sane R. P. Saxena P. K. Srivastava 《International journal of quantum chemistry》1982,21(6):1051-1055
When a Padé-type function is used as a trial function, it is necessary to investigate the location of singularities and the zeros of the optimized function. It is shown that an unacceptable wave function can sometimes yield numerically acceptable values because of the nature of the integration procedure. It is also shown that it is possible to remove the undesirable features of a lower order form by invoking the next approximation. 相似文献
8.
Anthony Jolly Dandan Miao Maxime Daigle Prof. Dr. Jean-François Morin 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(12):4652-4661
The solution-phase synthesis is one of the most promising strategies for the preparation of well-defined graphene nanoribbons (GNRs) in large scale. To prepare high quality, defect-free GNRs, cycloaromatization reactions need to be very efficient, proceed without side reaction and mild enough to accommodate the presence of various functional groups. In this Minireview, we present the latest synthetic approaches for the synthesis of GNRs and related structures, including alkyne benzannulation, photochemical cyclodehydrohalogenation, Mallory and Pd- and Ni-catalyzed reactions. 相似文献
9.
Anthony Jolly Dandan Miao Maxime Daigle Jean‐Franois Morin 《Angewandte Chemie (International ed. in English)》2020,59(12):4624-4633
The solution‐phase synthesis is one of the most promising strategies for the preparation of well‐defined graphene nanoribbons (GNRs) in large scale. To prepare high quality, defect‐free GNRs, cycloaromatization reactions need to be very efficient, proceed without side reaction and mild enough to accommodate the presence of various functional groups. In this Minireview, we present the latest synthetic approaches for the synthesis of GNRs and related structures, including alkyne benzannulation, photochemical cyclodehydrohalogenation, Mallory and Pd‐ and Ni‐catalyzed reactions. 相似文献
10.
The isomeric compounds 1 and 3, which differ only in the position of a methyl substituent, give opposite chemoselectivities in an esterase-catalyzed hydrolysis reaction. The esterase was chemoselective for the oxoester in 1, but for the thiol ester group in 3. A high enantioselectivity was observed for both 1 and 3. 相似文献