Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Ching-Shiang Fang"'
Publikováno v:
Journal of the Chinese Chemical Society. 67:2163-2170
Publikováno v:
Journal of Cluster Science. 30:1185-1193
In our attempts to identify probable intermediates in the preparation of anionic silver hydride cluster [Ag8(H){S2CC(CN)2}6]5− under the condition of excess NaBH4, we isolated and analyzed a new cluster compound, namely, [Bu4N]6[Ag7(H){S2CC(CN)2}6]
Autor:
Jean-Yves Saillard, Hao-Wei Chang, Samia Kahlal, Ruei-Yi Shiu, Ching-Shiang Fang, Jian-Hong Liao, Pilli V. V. N. Kishore, Chen-Wei Liu
Publikováno v:
Journal of Cluster Science
Journal of Cluster Science, Springer Verlag, 2017, 28 (2), pp.679--694. ⟨10.1007/s10876-016-1076-x⟩
Journal of Cluster Science, 2017, 28 (2), pp.679--694. ⟨10.1007/s10876-016-1076-x⟩
Journal of Cluster Science, Springer Verlag, 2017, 28 (2), pp.679--694. ⟨10.1007/s10876-016-1076-x⟩
Journal of Cluster Science, 2017, 28 (2), pp.679--694. ⟨10.1007/s10876-016-1076-x⟩
International audience; Two luminescent, monoanionic chalcogenide-centered nonanuclear silver clusters stabilized by dichalcogenophosphates were synthesized and fully characterized by various spectroscopies including multinuclear NMR and ESI-mass. Si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c314e057f8fc3667fc75316cd0eb5b3
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01515160
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01515160
Autor:
Ching-Shiang Fang, Werner E. van Zyl, Yi-Juan Li, Hao-Wei Chang, Bijay Sarkar, Chen-Wei Liu, Jian-Hong Liao
Publikováno v:
Dalton Trans.. 43:12380-12389
We report on a Ag5 coordination polymer and discrete Ag8 and Ag10 dithiophosphate clusters. The cluster formation and structures were affected by the stoichiometric control of the M : L molar ratios used. The cluster [Ag5{S2P(O(i)Pr)2}4]n(PF6)n, , is
Autor:
Chen-Wei Liu, Ping-Kuei Liao, Eric Furet, Ching-Shiang Fang, Camille Latouche, Jérôme Cuny, Jean-Yves Saillard, Yan-Ru Lin, Samia Kahlal
Publikováno v:
Inorganic Chemistry
Inorganic Chemistry, American Chemical Society, 2013, 52 (13), pp.7752-7765. ⟨10.1021/ic400959a⟩
Inorganic Chemistry, 2013, 52 (13), pp.7752-7765. ⟨10.1021/ic400959a⟩
Inorganic Chemistry, American Chemical Society, 2013, 52 (13), pp.7752-7765. ⟨10.1021/ic400959a⟩
Inorganic Chemistry, 2013, 52 (13), pp.7752-7765. ⟨10.1021/ic400959a⟩
International audience; M8L6 clusters (M = Cu(I), Ag(I); L = dichalcogeno ligand) are known for their ability to encapsulate various kinds of saturated atomic anions. Calculations on the models [M8(E2PH2)6]2+ (M = Cu(I), Ag(I); E = S, Se) and the ion
Autor:
Hong-Chih You, Ling-Song Chiou, Ching-Shiang Fang, C. W. Liu, Vladimir A. Kuimov, Ping-Kuei Liao
Publikováno v:
European Journal of Inorganic Chemistry. 2013:2083-2092
The reactions of the neutral phosphonoselenoate [Cp(CO)2FeP(Se)(OiPr)2] (1) with Lewis acids (GaCl3, InCl3) produce dicationic complexes [{Cp(CO)2FeP(OiPr)2}2Sen][GaCl4]2, [n = 2 (2), 3 (3)] and [{Cp(CO)2FeP(OiPr)2}2Sen][InCl4]2 [n = 2 (4), 3 (5)] in
Publikováno v:
Inorganic Chemistry
Inorganic Chemistry, 2013, 52, pp.2070-2077. ⟨10.1021/ic302482p⟩
Inorganic Chemistry, American Chemical Society, 2013, 52, pp.2070-2077. ⟨10.1021/ic302482p⟩
Inorganic Chemistry, 2013, 52, pp.2070-2077. ⟨10.1021/ic302482p⟩
Inorganic Chemistry, American Chemical Society, 2013, 52, pp.2070-2077. ⟨10.1021/ic302482p⟩
Reactions of Ag(I) salt, NH(4)(E(2)P(OR)(2)) (R = (i)Pr, Et; E = Se, S), and NaBH(4) in a 7:6:1 ratio in CH(2)Cl(2) at room temperature, led to the formation of hydride-centered heptanuclear silver clusters, [Ag(7)(H){E(2)P(OR)(2)}(6)] (R = (i)Pr, E
Publikováno v:
Journal of the Chinese Chemical Society. 59:480-484
The formation of a C-N bond via the cross-couplings of aryl iodides with azoles, aryl amine, and amides can be successfully achieved in decent yield by the utilization of both [Cu8(H){S2P(O i Pr)2}6] + and [Cu8{S2P(OEt)2}6] 2+ as the pre-catalysts.
Publikováno v:
Organometallics. 28:4958-4963
The organoiron-substituted phosphine selenides Cp(CO)2FeP(Se)(OR)2 (R = iPr (1a), nPr (1b), Et (1c)) were synthesized. The metalloligands, capable of reacting as nucleophiles toward Me3OBF4, formed Se-methylated products (2a−c). Upon reaction with
Publikováno v:
Journal of Organometallic Chemistry. 694:404-410
Mononuclear complexes of the type, M(CO)4[Se2P(OR)2] (M = Mn, R = iPr, 1a; Et, 1b; M = Re, R = iPr, 3a; Et, 3b) can be prepared from either [ -Se ( Se ) P ( O i Pr ) 2 ] 2 (A) or [Se{-Se(Se)P(OEt)2}2] (B) with M(CO)5Br. O,O′-dialkyl diselenophospha