Screening of metal complex catalysts using bidentate Schiff base ligands for controlled cationic polymerization of vinyl ethers using in situ complexation method

2019 ◽  
Vol 10 (30) ◽  
pp. 4209-4219 ◽  
Author(s):  
Sensho Kigoshi ◽  
Arihiro Kanazawa ◽  
Shokyoku Kanaoka ◽  
Sadahito Aoshima

Appropriate ligand scaffolds in cationic polymerization were screened using various bidentate Schiff base ligand/ZrCl4 initiating systems.

2014 ◽  
Vol 43 (37) ◽  
pp. 13831-13834 ◽  
Author(s):  
Yuan Dai ◽  
Yin-Ge Wang ◽  
Jiao Geng ◽  
Yu-Xin Peng ◽  
Wei Huang

A dinuclear Cu(ii) complex 3, having an unprecedented in situ formed 2,6-piperidin-4-one-based ligand produced from a flexible Schiff-base ligand HL1, can be yielded as a side product in Cu(OAc)2·H2O–NH3·H2O dissolved in methanol–acetone besides the expected dinuclear Cu(ii) complex 1.


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.


2021 ◽  
Author(s):  
SOUMYA SUNDAR MATI ◽  
Dr. SAUGATA KONAR ◽  
BOBY SAMAI

A zinc coordinated rare binuclear complex was synthesised and characterized by elemental analysis and single-crystal X-ray diffraction. Two mononuclear units formed by two Schiff base ligands 2-((2-(pyrimidin-2-yl)hydrazono)methyl)phenol (PHP) coordinated with...


2017 ◽  
Vol 46 (37) ◽  
pp. 12500-12506 ◽  
Author(s):  
A. Poma ◽  
A. Forni ◽  
C. Baldoli ◽  
P. R. Mussini ◽  
A. Bossi

Unexpected cis/trans isomerism in a bis-cyclometalated Pt(ii) complex is investigated by NMR, X-ray diffraction, optical, electrochemical and computational methods and rationalized.


2009 ◽  
Vol 64 (4) ◽  
pp. 403-408 ◽  
Author(s):  
Shyamapada Shit ◽  
Joy Chakraborty ◽  
Brajagopal Samanta ◽  
Georgina M. Rosair ◽  
Samiran Mitra

A new centrosymmetric trinuclear Zn(II) complex [Zn3L2(CH3COO)4] (1) has been synthesized by the reaction of Zn(CH3COO)2 · 2H2O with a tridentate N,N,O-donor Schiff base ligand HL [C5H4NC(CH3)=NC6H4(OH)] and systematically characterized by elemental analysis, FT-IR, UV/Vis and thermal methods. Single crystal X-ray structure analysis reveals that three Zn(II) centers are in two different coordination environments. Two terminal Zn(II) centers adopt a distorted squarepyramidal geometry leaving the central Zn(II) in a distorted octahedral environment. Two adjacent metal centers are connected through single μ2-phenolato as well as double μ-acetato-O,O´ syn-syn bridges. Fluorescence properties of the complex as compared to the ligand indicate that the former can serve as a potential photoactive material.


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