Dynamic functionalised metallogel: An approach to immobilised catalysis with improved activity
摘要:
A metal-organic gel (MOG) route to immobilised catalysts has been developed based on the reversibility of coordination bond formation in a Fe3+-carboxylate MOG. The ferric gel was rationally designed based on a bifunctional ligand, 5-1H-benzo[d]imidazole-1,3-dicarboxylic acid (L1), in which the imidazole N atom may further hind to a soft ion like Pd2+ more strongly Clue to the HSAB matching. Palladium(II) was successfully loaded in the gel to yield a supported coordination catalyst. Compared with its homogeneous counterparts, the immobilised gel catalyst exhibited significantly improved catalytic activity Under mild conditions as shown in Suzuki-Miyaura C-C coupling, and Could be reused for several times. (C) 2009 Elsevier B.V. All rights reserved.
[EN] SUBSTITUTED INDOLE MCL-1 INHIBITORS<br/>[FR] INHIBITEURS DE INDOLE MCL-1 SUBSTITUÉS
申请人:UNIV VANDERBILT
公开号:WO2015148854A1
公开(公告)日:2015-10-01
The present invention provides for compounds that inhibit the activity of an anti-apoptotic Bcl-2 family member Myeloid cell leukemia-1 (Mcl-1) protein. The present invention also provides for pharmaceutical compositions as well as methods for using compounds for treatment of diseases and conditions (e.g., cancer) characterized by the over-expression or dysregulation of Mcl-1 protein.
Palladium dichloride adduct of N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine: synthesis, structure and catalytic performance in the decarboxylative cross-coupling of 4-picolinic acid with aryl bromide
作者:Run-Tian He、Jian-Feng Wang、Hui-Fang Wang、Zhi-Gang Ren、Jian-Ping Lang
DOI:10.1039/c4dt00815d
日期:——
Reaction of PdCl2 with N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine (bdppmapy) afforded a mononuclear complex [(bdppmapy)PdCl2] (1). Compound 1 was characterized by elemental analysis, IR, 1H, 13C and 31P NMR, electrospray ion mass spectra (ESI-MS) and X-ray single crystal crystallography. The Pd(II) center in 1 is chelated by bdppmapy, showing a cis-square planar geometry. With the assistance of additive Cu2O, complex 1 exhibited good catalytic activity toward the decarboxylative cross-coupling reactions between 4-picolinic acid and aryl bromides. In the presence of only 2 mol% catalyst, a family of 4-aryl-pyridines could be isolated in up to 83% yield.
Chromophoric Lewis Base Adducts of Methyltrioxorhenium: Synthesis, Catalysis and Photochemistry
作者:Simone A. Hauser、Valentina Korinth、Eberhardt Herdtweck、Mirza Cokoja、Wolfgang A. Herrmann、Fritz E. Kühn
DOI:10.1002/ejic.201000348
日期:2010.9
A series of chromophoricLewisbaseadducts of methyltrioxorhenium (MTO) was examined. The ligands were pyridine derivatives with different size of the aromatic system and variable substituents, thus providing a variation of electronic and steric parameters. The complexes were fully characterised (UV/Vis, IR and NMR spectroscopy, single-crystal X-ray diffraction and elemental analysis) and their stability
研究了一系列甲基三氧铼 (MTO) 的发色路易斯碱加合物。配体是具有不同大小的芳香系统和可变取代基的吡啶衍生物,因此提供了电子和空间参数的变化。对配合物进行了充分表征(UV/Vis、IR 和 NMR 光谱、单晶 X 射线衍射和元素分析),并通过 UV/Vis 光谱测定了它们在二氯甲烷中的稳定性常数。此外,本报告还研究了与 MTO 配位的这些 N-供体配体对 1-辛烯环氧化催化活性的影响。每个化合物测试两次;在避光和日光下进行催化反应。未发现催化性能有显着差异。通过 (17)O-NMR 和 UV/Vis 光谱研究了配合物在紫外光照射下的行为。本文公开的实验旨在探讨 MTO 加合物中发色 N 供体配体的潜在有益作用,因为它们可能通过提供额外的能量来削弱在催化循环中必须断裂的键来激活催化系统。
CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME
申请人:SAMSUNG DISPLAY CO., LTD.
公开号:US20170077422A1
公开(公告)日:2017-03-16
An organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer, wherein the organic layer includes at least one condensed cyclic compound of Formula 1:
An organic light-emitting device including the condensed cyclic compound according to embodiments of the present disclosure may have low driving voltage, high efficiency, high luminance, and long lifespan.
The present invention provides for compounds that inhibit the activity of an anti-apoptotic Bcl-2 family member Myeloid cell leukemia-1 (Mcl-1) protein. The present invention also provides for pharmaceutical compositions as well as methods for using compounds for treatment of diseases and conditions (e.g., cancer) characterized by the over-expression or dysregulation of Mcl-1 protein.