Zobrazeno 1 - 10
of 777
pro vyhledávání: '"Alan L. Balch"'
Publikováno v:
ACS Omega, Vol 6, Iss 31, Pp 20321-20330 (2021)
Externí odkaz:
https://doaj.org/article/1e55f5fdd3bf422fb827e3071319f7bd
Autor:
James C. Duchamp, Harry C. Dorn, Aleksander L. Wysocki, Kyungwha Park, Marilyn M. Olmstead, Mrittika Roy, Alan L. Balch
Publikováno v:
Inorganic Chemistry. 62:5114-5122
Autor:
Daniel T. Walters, Michael M. Aristov, Reza Babadi Aghakhanpour, Daniel J. SantaLucia, Sarah Costa, Marilyn. M. Olmstead, John F. Berry, Alan. L. Balch
Publikováno v:
Inorganic Chemistry. 62:4467-4475
Publikováno v:
Crystal Growth & Design. 23:915-922
Autor:
Nicolas Cena, Andrew J. Peloquin, Jerry A. Boatz, Sarah Costa, Steven R. Gralinski, Alan L. Balch, Kamran B. Ghiassi
Publikováno v:
Chemical Communications. 58:11673-11676
1,2-Diphenylhydrazine rearranges to ortho-semidine upon reaction with RuCl2(PPh3)3. Crystals of two polymorphs show chiral resolution, producing an enantiopure form, in addition to a racemic, “disappearing” form.
Publikováno v:
New Journal of Chemistry. 46:6663-6669
Pyrazole-, isoxazole- and pyrrole-ring fused derivatives of C60.
Publikováno v:
Chemical Communications. 57:10218-10221
Treatment of an open-cage fullerene, designated as MMK-9, with (Ph3P)4Pt in toluene solution at room temperature allows a (PPh3)2Pt unit to be incorporated into the rim of the cage so that it becomes an integral part of the carbon cage skeleton. The
Autor:
Christopher D. Lowe, Marilyn M. Olmstead, Alan L. Balch, Venoos Moshayedi, Lucy M. C. Luong, Alexandria V. Adams
Publikováno v:
Chemical Science
Chemical science, vol 11, iss 43
Chemical science, vol 11, iss 43
Non-luminescent, isostructural crystals of [(C6H11NC)2Au](EF6)·C6H6 (E = As, Sb) lose benzene upon standing in air to produce green luminescent (E = As) or blue luminescent (E = Sb) powders. Previous studies have shown that the two-coordinate cation
Publikováno v:
Chemistry – A European Journal. 28
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(17)
Direct synthesis of diamine radical cations in crystalline form proceeding through oxidation of triphenylamine followed by the formation of a new C-N bond is reported. Although the oxidative coupling of triphenylamine is well studied, diamine product