Efficient in situ three-component formation of chiral oxazoline-Schiff base copper(ii) complexes: towards combinatorial library of chiral catalysts for asymmetric Henry reaction

2010 ◽  
Vol 8 (13) ◽  
pp. 2956 ◽  
Author(s):  
Wen Yang ◽  
Han Liu ◽  
Da-Ming Du
Author(s):  
Shabana Noor ◽  
Richard Goddard ◽  
Fehmeeda Khatoon ◽  
Sarvendra Kumar ◽  
Rüdiger W. Seidel

AbstractSynthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes with the formula [ZnLn(HL)(µ-OAc)(NO3)2(H2O)x(MeOH)1-x]NO3 · n H2O · n MeOH [Ln = Pr (1), Nd (2)] and the crystal and molecular structure of [ZnNd(HL)(µ-OAc)(NO3)2(H2O)] [ZnNd(HL)(OAc)(NO3)2(H2O)](NO3)2 · n H2O · n MeOH (3) are reported. The asymmetrical compartmental ligand (E)-2-(1-(2-((2-hydroxy-3-methoxybenzylidene)amino)-ethyl)imidazolidin-2-yl)-6-methoxyphenol (H2L) is formed from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation, resulting in a peripheral imidazoline ring. The structures of 1–3 were revealed by X-ray crystallography. The smaller ZnII ion occupies the inner N2O2 compartment of the ligand, whereas the larger and more oxophilic LnIII ions are found in the outer O2O2’ site. Graphic Abstract Synthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes (Ln = Pr, Nd) bearing an asymmetrical compartmental ligand formed in situ from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation are reported.


RSC Advances ◽  
2017 ◽  
Vol 7 (28) ◽  
pp. 17005-17019 ◽  
Author(s):  
Shifeng Yan ◽  
Taotao Wang ◽  
Xing Li ◽  
Yuhang Jian ◽  
Kunxi Zhang ◽  
...  

The in situ forming hydrogels based on oppositely charged poly(l-glutamic acid) (PLGA) and chitosan (CS) were prepared via a Schiff base crosslinking reaction.


Author(s):  
Fan Xu ◽  
Xue-Jing Luo ◽  
Cui-E Wu ◽  
Bei-Yi Liao ◽  
Kai Wang ◽  
...  

2019 ◽  
Vol 254 ◽  
pp. 194-197 ◽  
Author(s):  
Atefeh Torabi ◽  
Maryam Sahraro ◽  
Mehdi Barikani ◽  
Hamed Daemi

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