scholarly journals Evaluation of a chiral cubane-based Schiff base ligand in asymmetric catalysis reactions

2012 ◽  
Vol 8 ◽  
pp. 1814-1818 ◽  
Author(s):  
Kyle F Biegasiewicz ◽  
Michelle L Ingalsbe ◽  
Jeffrey D St. Denis ◽  
James L Gleason ◽  
Junming Ho ◽  
...  
Keyword(s):  
Schiff Base ◽  
Asymmetric Catalysis ◽  
Schiff Base Ligand ◽  
Membered Ring ◽  
Addition Reactions ◽  
Henry Reaction ◽  
Organic Transformations ◽  
Computational Evaluation ◽  
Copper Center ◽  
B3lyp Calculations

Recently, a novel chiral cubane-based Schiff base ligand was reported to yield modest enantioselectivity in the Henry reaction. To further explore the utility of this ligand in other asymmetric organic transformations, we evaluated its stereoselectivity in cyclopropanation and Michael addition reactions. Although there was no increase in stereocontrol, upon computational evaluation using both M06L and B3LYP calculations, it was revealed that a pseudo six-membered ring exists, through H-bonding of a cubyl hydrogen to the copper core. This decreases the steric bulk above the copper center and limits the asymmetric control with this ligand.

Adsorption and Separation of Organic Six-Membered Ring Analogues on Neutral Cd(II)-MOF Generated from Asymmetric Schiff-Base Ligand

2010 ◽  
Vol 49 (23) ◽  
pp. 11164-11173 ◽  
Author(s):  
Li Duan ◽  
Zhen-Hua Wu ◽  
Jian-Ping Ma ◽  
Xiang-Wen Wu ◽  
Yu-Bin Dong
Keyword(s):  
Schiff Base ◽  
Schiff Base Ligand ◽  
Membered Ring

Spin-crossover in an iron(iii) complex showing a broad thermal hysteresis

2021 ◽  
Author(s):  
Cyril Rajnák ◽  
Romana Mičová ◽  
Ján Moncoľ ◽  
Ľubor Dlháň ◽  
Christoph Krüger ◽  
...  
Keyword(s):  
Schiff Base ◽  
Schiff Base Ligand ◽  
Spin Crossover ◽  
Thermal Hysteresis ◽  
Mononuclear Complex ◽  
Hysteresis Width ◽  
Thermally Induced

A pentadentate Schiff-base ligand 3,5Cl-L2− and NCSe− form a iron(iii) mononuclear complex [Fe(3,5Cl-L)(NCSe)], which shows a thermally induced spin crossover with a broad hysteresis width of 24 K between 123 K (warming) and 99 K (cooling).

Schiff Base Metal Complexes Precursor for Metal Oxide Nanomaterial: A Review

2020 ◽  
Vol 16 ◽  
Author(s):  
Meghshyam K. Patil ◽  
Vijay H. Masand ◽  
Atish K. Maldhure
Keyword(s):  
Schiff Base ◽  
Metal Complexes ◽  
Metal Oxides ◽  
Base Metal ◽  
Carbonyl Compounds ◽  
Organic Transformations ◽  
Iron Cobalt ◽  
Methods Of Synthesis ◽  
Schiff Base Metal Complexes ◽  
Nickel Manganese

: Schiff bases and their complexes are versatile compounds, which have been synthesized from the condensation of carbonyl compounds with amino compounds and exhibit a broad range of applications in biological, medicinal, catalysis, and industrial purposes. Furthermore, Schiff base-metal complexes have been used as a precursor for the synthesis of different metal oxides, which includes oxides of iron, cobalt, copper, nickel, manganese, vanadium, cadmium, zinc, mercury, etc. and ferrites such as Fe3O4, ZnFe2O4, and ZnCo2O4. These metal oxides have been utilized for several applications, which includes as a catalyst for several organic transformations and for biological activity. This review encompasses different methods of synthesis of metal oxides using Schiff base metal complexes precursor, their characterization, and various applications in detail.

A facile synthesized benzophenone Schiff-base ligand as efficient type II visible light photoinitiator

2021 ◽  
Vol 157 ◽  
pp. 106329
Author(s):  
Tanlong Xue ◽  
Yang Li ◽  
Xiangchen Zhao ◽  
Jun Nie ◽  
Xiaoqun Zhu
Keyword(s):  
Schiff Base ◽  
Visible Light ◽  
Schiff Base Ligand ◽  
Type Ii ◽  
Efficient Type

DNA cleavage mechanism by metal complexes of Cu(II), Zn(II) and VO(IV) with a schiff-base ligand

Biochimie ◽  
2021 ◽  
Vol 186 ◽  
pp. 43-50
Author(s):  
María R. Rodríguez ◽  
Martín J. Lavecchia ◽  
Beatriz S. Parajón-Costa ◽  
Ana C. González-Baró ◽  
María R. González-Baró ◽  
...  
Keyword(s):  
Schiff Base ◽  
Metal Complexes ◽  
Schiff Base Ligand ◽  
Dna Cleavage

scholarly journals Structural Characterization of Heterodinuclear ZnII-LnIII Complexes (Ln = Pr, Nd) with a Ring-Contracted H2valdien-Derived Schiff Base Ligand

2021 ◽  
Author(s):  
Shabana Noor ◽  
Richard Goddard ◽  
Fehmeeda Khatoon ◽  
Sarvendra Kumar ◽  
Rüdiger W. Seidel
Keyword(s):  
Molecular Structure ◽  
Schiff Base ◽  
Structural Characterization ◽  
Schiff Base Ligand ◽  
Crystal And Molecular Structure ◽  
X Ray ◽  
X Ray Crystallography ◽  
Imidazoline Ring

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.

scholarly journals Schiff base ligand L synthesis and its evaluation as anticancer and antidepressant agent

2020 ◽  
pp. 101331
Author(s):  
Maria Sadia ◽  
Jehangir Khan ◽  
RobinaNaz ◽  
Muhammad Zahoor ◽  
Syed Wadood Ali Shah ◽  
...  
Keyword(s):  
Schiff Base ◽  
Schiff Base Ligand ◽  
Antidepressant Agent
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