- Inorganic organic hybrid material with high water stability as well as blue-green emission light and photoelectric response performance
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The invention discloses an inorganic organic hybrid material with high water stability as well as blue-green emission light and photoelectric response performance. The inorganic organic hybrid material is prepared by taking silver bromide, 1,2di triphenylphosphine bromoethane (1,2-DBTPP.2Br) as reaction raw materials and adopting a simple solution volatilization method. The inorganic organic hybrid material has good water stability, shows blue-green emission light and good photoelectric response performance (light current is 0.17 Ua), and can be used for light emission and optoelectronic switch devices in a liquid phase system; in addition, the inorganic organic hybrid material has the advantages of low preparation cost, simple operation method and high yield.
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Paragraph 0023
(2019/08/01)
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- Evaluation of bifunctional chiral phosphine oxide catalysts for the asymmetric hydrosilylation of ketimines
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A series of bifunctional phosphine oxides have been prepared and evaluated as catalysts for the trichlorosilane mediated asymmetric hydrosilylation of ketimines. bis-Phosphine oxides, hydroxy-phosphine oxides, and biaryl phosphine oxides all demonstrated good catalytic activity, but poor to moderate enantioselectivity. A bis-P-chiral phosphine oxide displayed the highest enantioselectivity of 60%.
- Warner, Christopher J.A.,Berry, Sian S.,Jones, Simon
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- ATP3 and MTP3: Easily Prepared Stable Perruthenate Salts for Oxidation Applications in Synthesis
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The Ley–Griffith tetra-n-propylammonium perruthenate (TPAP) catalyst has been widely deployed by the synthesis community, mainly for the oxidation of alcohols to aldehydes and ketones, but also for a variety of other synthetic transformations (e.g. diol cleavage, isomerizations, imine formation and heterocyclic synthesis). Such popularity has been forged on broad reaction scope, functional group tolerance, mild conditions, and commercial catalyst supply. However, the mild instability of TPAP creates preparation, storage, and reaction reproducibility issues, due to unpreventable slow decomposition. In search of attributes conducive to catalyst longevity an extensive range of novel perruthenate salts were prepared. Subsequent evaluation unearthed a set of readily synthesized, bench stable, phosphonium perruthenates (ATP3 and MTP3) that mirror the reactivity of TPAP, but avoid storage decomposition issues.
- Moore, Peter W.,Read, Christopher D. G.,Bernhardt, Paul V.,Williams, Craig M.
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supporting information
p. 4556 - 4561
(2018/03/13)
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- Special features of the interaction of pyridine and quinoline derivatives, and related compounds with triphenylphosphine
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Using pyridine, quinoline, and related compounds as examples, it has been shown that their interaction with triphenylphosphine occurs via different pathways. Reaction of triphenylphosphine with N-vinylisonicotinic acid chloride leads to the mixture of 1,2
- Khachikyan,Simonyan,Manukyan,Indzhikyan
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p. 1359 - 1364
(2013/09/23)
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- Features of the reaction of 2,3-dihalopropanoic acids with pyridines and nucleophilic addition to N-vinylpyridinium salts
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The example of vinylpyridinium salts to establish for the first time the possibility of nucleophilic addition to the vinyl group in quaternary ammonium salts, which provides evidence against the concept that such reactions involve d orbitals. The nucleoph
- Khachikyan, R. Dzh.,Davtyan,Indzhikyan
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experimental part
p. 1452 - 1457
(2009/02/07)
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- Properties of onium salts of phosphorus and nitrogen
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Ammonium and phosphonium halides when heated with excess dimethyl or diethyl phosphite can undergo anion exchange as a result of alkylation of halide ions with dialkyl phosphites. Experimental data were obtained, that cast some doubt in the commonly accepted opinion that reactions of tertiary amines and phosphines with dihalides in apolar media result in exclusive formation of monosalts. 2005 Pleiades Publishing, Inc.
- Ovakimyan,Barsegyan,Kikoyan,Indzhikyan
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p. 1074 - 1076
(2007/10/03)
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- Understanding the structural properties of a homologous series of bis-diphenylphosphine oxides
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A homologous series of bis-diphenylphosphine oxides (C6H5)2PO-(CH2)nPO(C 6H5)2 (with n = 2-8; denoted 2-8] have been investigated to explore the effects of a range of competing and cooperative intermolecular and intramolecular interactions on the structural properties in the solid state. The important factors influencing the structural properties include intramolecular aspects such as the conformation of the aliphatic chain and the intramolecular interaction between the two P=O dipoles in the molecule, and intermolecular aspects such as long-range electrostatic interactions (dominated by the arrangement of the P=O dipoles), C-H ... O interactions, C-H ... π interactions and π ... π interactions. Compounds 3 and 5 could be crystallized only as solvate co-crystals (3 · water and 5 · (toluene)2], whereas the crystal structures of all the other compounds contain only the bis-diphenylphosphine oxide molecule. The crystal structures have been determined from single-crystal X-ray diffraction data, with the exception of 7 (which has been determined here from powder X-ray diffraction data) and 4 (which was known previously). The compounds with even n represent a systematic structural series, exhibiting characteristic, essentially linear P=O ... P=O ... P=O dipolar arrays, together with C-H ... O and C-H ... π interactions. For the compounds with odd n, on the other hand, uniform structural behaviour is not observed across the series, although certain aspects of these crystal structures contribute in a general sense to our understanding of the structural properties of bis-diphenylphosphine oxides. Importantly, for the compounds with odd n, there is "frustration" with regard to the molecular conformation, as the preferred all-anti conformation of the aliphatic chain gives rise to an unfavourable parallel alignment of the two P=O dipoles within the molecule. Clearly the importance of avoiding a parallel alignment of the P=O dipoles becomes greater as n decreases. Local structural aspects (investigated by high-resolution solid-state 31P NMR spectroscopy) and thermal properties of the bis-diphenylphosphine oxide materials are also reported.
- Calcagno, Patrizia,Kariuki, Benson M.,Kitchin, Simon J.,Robinson, James M. A.,Philp, Douglas,Harris, Kenneth D. M.
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p. 2338 - 2349
(2007/10/03)
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- SYNTHESE DE SELS DE VINYLPHOSPHONIUMS β-SUBSTITUES ET DE SELS D'ALKYLPHOSPHONIUMS β-DISUBSTITUES
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Vinylene-1,2 bisphosphoniums salts react, in the presence of a base, with compounds ZH having a mobile hydrogen, to give a way of sysnhesis of β-substituted vinylphosphoniums salts 2 or β-disubstituted alkylphosphoniums salts 3.We have studied the limits of these synthesis depending on the experimental conditions and the nature of compounds ZH (alcohols, phenols, thiols, phosphines, amines).
- Cristau, Henri-Jean,Bottaro, Denis,Plenat, Francoise,Pietrasanta, Francine,Christol, Henri
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