91569-39-0Relevant articles and documents
Synthesis, crystal structure and luminescence properties of lanthanide coordination polymers with a new semirigid bridging thenylsalicylamide ligand
Song, Xue-Qin,Wang, Li,Zhao, Meng-Meng,Wang, Xiao-Run,Peng, Yun-Qiao,Cheng, Guo-Quan
, p. 183 - 189 (2013)
Two new lanthanide coordination polymers based on a semirigid bridging thenylsalicylamide ligand {[Ln2L3(NO3) 6]] (C4H8O2)2}∞ were obtained and characterized by elemen
Lanthanide coordination polymers constructed by a new semirigid bridging salicylamide ligand: Synthesis, structure and luminescence properties
Song, Xue-Qin,Wang, Li,Zhao, Meng-Meng,Cheng, Guo-Quan,Wang, Xiao-Run,Peng, Yun-Qiao
, p. 71 - 77 (2013)
A new semirigid exo-bidentate ligand incorporating thenylsalicylamide terminal groups, namely 1,4-bis{[(2′-thenylaminoformyl)phenoxyl]methyl}-2, 5-bismethylbenzene was synthesized and used as building blocks for constructing lanthanide coordination polymers with luminescent properties. The series of lanthanide nitrate complexes have been characterized by elemental analysis, IR spectroscopy, and X-ray diffraction analysis. All the lanthanide coordination polymers exhibit the same metal-to-ligand molar ratio of 2:3 and the semirigid exo-bidentate ligand as a bridging ligand, reacts with lanthanide nitrates forming 1D annular chains {[Ln2(NO3)6L 3.2013 Elsevier B.V. All rights reserved.
Synthesis and crystal structure of 1,4-bis{[(2'-Thenylaminoformyl)phenoxyl] methyl}benzene
Wang, Li,Wang, Xiao-Run,Cheng, Guo-Quan,Peng, Yun-Qiao,Song, Xue-Qin
, p. 10004 - 10006 (2014/01/06)
A novel salicylamide derivative i.e., 1,4-bis{[(2'-thenylaminoformyl) phenoxyl]methyl}benzene with the m.f. C32H28N 2O4S2 has been synthesized and the crystal structure was determined by single crystal X-ray diffraction. There are strong intramolecular hydrogen bonding between the amide nitrogen atoms and the ethereal oxygen atoms which stabilized the structure to form a trans configuration. Furthermore the title compound are linked by intermolecular C9-H9O1 hydrogen bonds into an infinite 1D chain parallel to the bc plane.
One-pot stibine modified Co2(CO)8 catalyzed reductive N-alkylation of primary amides with carbonyl compounds
Rubio-Pérez, Laura,Sharma, Pankaj,Pérez-Flores, F. Javier,Velasco, Luis,Arias, J. Luis.,Cabrera, Armando
experimental part, p. 2342 - 2348 (2012/04/10)
A one-pot stibine modified Co2(CO)8 homogeneous catalytic reductive N-alkylation of primary amides using aldehydes/ketones as alkylating agents, is reported. Good to excellent yields of a wide range of secondary amides are obtained (up to 97%) under relative mild conditions.