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pro vyhledávání: '"35"'
Publikováno v:
Journal of the American Chemical Society
The use of porous materials to store natural gas in vehicles requires large amounts of methane per unit of volume. Here we report the synthesis, crystal structure and methane adsorption properties of two new aluminum metal-organic frameworks, MOF-519
Autor:
Ryan W. Mills, Aaron J. Rossini, Graham A. Briscoe, Jochen Autschbach, Stephen J. Geier, Shaohui Zheng, Robert W. Schurko, Ivan Hung, Erin L. Norton
Publikováno v:
Journal of the American Chemical Society. 131(9)
Static solid-state (35)Cl (I = (3)/(2)) NMR spectra of the organometallic compounds Cp(2)TiCl(2), CpTiCl(3), Cp(2)ZrCl(2), Cp(2)HfCl(2), Cp*(2)ZrCl(2), CpZrCl(3), Cp*ZrCl(3), Cp(2)ZrMeCl, (Cp(2)ZrCl)(2)mu-O, and Cp(2)ZrHCl (Schwartz's reagent) have b
Publikováno v:
Wilting, J, Janssen, M H M, Muller, C J & Vogt, D 2006, ' The enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene ', Journal of the American Chemical Society, vol. 128, no. 35, pp. 11374-5 . https://doi.org/10.1021/ja064378u
Journal of the American Chemical Society, 128(35), 11374-11375. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-5. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-11375. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-5. American Chemical Society
On the basis of deuterium labeling experiments and an equal 1,2-/1,4-product distribution, the reductive elimination of the product has been established to be the enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene. Thi
Publikováno v:
Journal of the American Chemical Society. 118:3643-3655
[N3N]TaPPh ([N3N]3- = [(Me3SiNCH2CH2)3N]3-) reacts with excess lithium metal in tetrahydrofuran to give “[N3N]TaPLi”, as judged by NMR studies and by reactions with RX at −35 °C to afford the phosphinidene complexes [N3N]TaPR (R = Me, n-Bu, Si
Publikováno v:
Journal of the American Chemical Society. 128(25)
Nickel complexes having a bulky tri(sec-alkyl)phosphine ligand catalyze hydroheteroarylation of alkynes at 35 degrees C. Selective activation of an Ar-H bond over an Ar-CN bond of N-protected 3-cyanoindoles is achieved by a proper choice of ligand an
Autor:
Adam S. Veige, Soumya Sarkar, Adam R. Carlson, Khalil A. Abboud, Joseph M. Falkowski, Melanie K. Veige
Publikováno v:
Journal of the American Chemical Society. 130:1116-1117
The new terphenyl pincer precursor 3,3‘ ‘-di-tert-butyl-1,1‘:3‘,1‘ ‘-terphenyl-2,2‘ ‘-diol (1) is examined for its ability to support early transition metals as a trianionic ligand. Metalation proceeds smoothly at −35 °C with Mo(NM
Publikováno v:
Journal of the American Chemical Society, 128(35), 11344-11345. American Chemical Society
We report the formation of high-precision catalysts using encapsulated rhodium complexes. In the current example, the encapsulated rhodium catalyst shows unprecedented high selectivity in the rhodium-catalyzed hydroformylation of internal alkenes, fo
Autor:
W. B. Reynolds, Gerard Kraus
Publikováno v:
Journal of the American Chemical Society. 72:5621-5626
The extent of additive and substitutive chlorination was determined for emulsion polyisoprene, Hevea and gutta-percha chlorinated to different chlorine contents in darkness and in a nitrogen atmosphere. The maximum amount of additive chlorine that ca