scholarly journals Tetranuclear Cu(ii)-chiral complexes: synthesis, characterization and biological activity

RSC Advances ◽  
2019 ◽  
Vol 9 (42) ◽  
pp. 24087-24091 ◽  
Author(s):  
Krisana Peewasan ◽  
Marcel P. Merkel ◽  
Kristof Zarschler ◽  
Holger Stephan ◽  
Christopher E. Anson ◽  
...  
Keyword(s):  
Biological Activity ◽  
Schiff Base ◽  
Single Crystal ◽  
Cd Spectroscopy ◽  
Schiff Base Complexes ◽  
X Ray Diffraction ◽  
Chiral Complexes ◽  
Enantiomerically Pure ◽  
X Ray

A pair of tetranuclear chiral Cu(ii)-Schiff-base complexes were synthesized using enantiomerically pure (S)-H2L and (R)-H2L ligands. These were characterised using single-crystal X-ray diffraction and CD spectroscopy and their biological activity tested.

scholarly journals H-bonded Chains and Networks: A Recurring Feature in the Solid State Structures of Manganese (III) Carboxylate Schiff Base Complexes

2013 ◽  
Vol 12 (2) ◽  
pp. 8-20
Author(s):  
Biny Sasi ◽  
Swathy S ◽  
Thampidas V S ◽  
Pike D Robert
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
Single Crystal ◽  
Schiff Base Complexes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Distorted Octahedral ◽  
Jahn Teller ◽  
Solid State Structures

Two new manganese(III) Schiff base complexes,  [Mn(salen)(m-NO2-C6H4CO2)(H2O)] (1) and  [Mn(msalen) (p-OH-C6H4CO2)(H2O)] (2), where H2salen = N,N'-bis(salicylidene)-1,2-diaminoethane, H2msalen = N,N'-bis (3-methoxysalicylidene)-1,2-diaminoethane were synthesized from the manganese (II) carboxylates.  Single crystal X-ray diffraction studies show that the Jahn-Teller distorted octahedral complexes are stabilized by              H-bonded chains and networks in the solid state.  

Steric influence of salicylaldehyde-based Schiff base ligands on the formation of trans-[Re(PR3)2(Schiff base)]+ complexes

2019 ◽  
Vol 48 (34) ◽  
pp. 12943-12955
Author(s):  
Jakob E. Baumeister ◽  
Andrew W. Mitchell ◽  
Steven P. Kelley ◽  
Charles L. Barnes ◽  
Silvia S. Jurisson
Keyword(s):  
Schiff Base ◽  
Single Crystal ◽  
Schiff Base Complexes ◽  
Steric Effects ◽  
X Ray Diffraction ◽  
Schiff Base Ligands ◽  
X Ray ◽  
Steric Influence

The steric effects of backbone groups on the synthesis and stability of trans-[Re(PR3)2(Schiff base)]+ compounds were assessed using NMR, HPLC, electrochemistry and single crystal X-ray diffraction.

scholarly journals A series of Mn(i) photo-activated carbon monoxide-releasing molecules with benzimidazole coligands: synthesis, structural characterization, CO releasing properties and biological activity evaluation

RSC Advances ◽  
2019 ◽  
Vol 9 (36) ◽  
pp. 20505-20512 ◽  
Author(s):  
Mixia Hu ◽  
YaLi Yan ◽  
Baohua Zhu ◽  
Fei Chang ◽  
Shiyong Yu ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Biological Activity ◽  
Activated Carbon ◽  
Fluorescence Spectroscopy ◽  
Single Crystal ◽  
Structural Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
H Nmr ◽  
C Nmr

Five Mn(i) photo-activated carbon monoxide-releasing molecules were synthesized by reactions of MnBr(CO)5 with L1–L4, and characterized via single crystal X-ray diffraction, 1H-NMR, 13C-NMR, IR, UV-vis and fluorescence spectroscopy.

Anti-mycobacterial activities of copper(II) salicylaldimine complexes derived from long-chain aliphatic amines

2013 ◽  
Vol 91 (11) ◽  
pp. 1093-1097 ◽  
Author(s):  
Alyssa E. Patterson ◽  
Eric G. Bowes ◽  
Allyson Bos ◽  
Taryn O’Neill ◽  
Haoxin Li ◽  
...  
Keyword(s):  
Mycobacterium Tuberculosis ◽  
Schiff Base ◽  
Aliphatic Amines ◽  
Schiff Base Complexes ◽  
Aliphatic Chain ◽  
X Ray Diffraction ◽  
X Ray ◽  
Microwave Assisted ◽  
Long Chain

Twelve copper(II) Schiff base complexes derived from lipophilic amines have been prepared using either salicylaldehyde or ortho-vanillin via a microwave-assisted reaction. All complexes have been obtained elementally pure and an X-ray diffraction of an isopentyl derivative has confirmed the structure of these compounds. All complexes showed a promising degree of anti-mycobacterial activity against Mycobacterium tuberculosis, where activity seemed to increase with an increase in the length of the aliphatic chain.

Synthesis, Characterization, and Antimicrobial Activities of New Organic-Inorganic Hybird Compound Based on Polyoxovanadate and Metal-Schiff-Base Complex

2015 ◽  
Vol 1105 ◽  
pp. 215-219
Author(s):  
Qiong Wu ◽  
Xiao Lin Ji ◽  
Lu Jing ◽  
Hong Ping Ju ◽  
Hai Wang
Keyword(s):  
Schiff Base ◽  
Human Cancer ◽  
Synergetic Effect ◽  
Schiff Base Complex ◽  
Antimicrobial Activities ◽  
Schiff Base Complexes ◽  
X Ray Diffraction ◽  
Base Complex ◽  
X Ray ◽  
Vis Spectroscopy

The reaction of polyoxovanadate and metal-Schiff base complex resulted in the formation of a new organic-inorganic hybrid compounds with the formula Na2[Mn (Salen)(H2O)2]4[V10O28]·9H2O (1) (salen=N,N’-ethylene-bis (salicylideneiminate). Compound 1 have been structurally characterized by IR, UV-vis spectroscopy and single crystal X-ray diffraction. Crystal data for 1: Triclinic, P-1, a=14.1123(3)Å, b=13.9397(7) Å, c=14.2564(5)Å, α=65.4160(9)°, β=81.3920(6)°, γ=89.5740(7) °. Structural analyses revealed that compound 1 represent a rare example of isopolyoxovanadate based metal-Schiff-base complexes, moreover, this is the first POM based metal Schiff-base complex isolated in aqueous solution medium, which may also propose a green chemical way to the synthesis of POM based hybrid. Compare with isopolyoxovanadate precusor Na6 [V10O28], compound 1 exhibit higher antimicrobial activities against human cancer cell, the phenomenon can be explained by the synergetic effect between POM and Schiff-base complex.

scholarly journals Synthesis, single crystal X-ray diffraction, Hirshfeld surface and biological activity of quinolone derivatives

2017 ◽  
Vol 8 (4) ◽  
pp. 422-429
Author(s):  
Huma Bano ◽  
Sarah Shafi ◽  
Hina Siddiqui ◽  
Muhammad Iqbal Choudhary ◽  
Sammer Yousuf
Keyword(s):  
Biological Activity ◽  
Single Crystal ◽  
Hirshfeld Surface ◽  
X Ray Diffraction ◽  
X Ray ◽  
Quinolone Derivatives

A Planar-Chiral Pillar[5]arene-Based Monophosphine Ligand with Induced Chirality at the Biaryl Axis

Synlett ◽  
2018 ◽  
Vol 29 (16) ◽  
pp. 2167-2170 ◽  
Author(s):  
Yuuya Nagata ◽  
Tomoki Ogoshi ◽  
Michinori Suginome ◽  
Yasuo Shimada ◽  
Tsuyoshi Nishikawa ◽  
...  
Keyword(s):  
Single Crystal ◽  
Diffraction Analysis ◽  
Asymmetric Catalysis ◽  
Cd Spectroscopy ◽  
Asymmetric Reactions ◽  
Side Chains ◽  
Chiral Ligand ◽  
X Ray Diffraction ◽  
Chirality Transfer ◽  
X Ray

A planar-chiral pillar[5]arene with cyclohexylmethoxy side chains and a pendant diphenylphosphine was prepared and used as a chiral ligand in asymmetric reactions. Chirality transfer from the planar-chiral pillar[5]arene scaffold to the chiral biaryl moiety was demonstrated by circular dichroism (CD) spectroscopy, single-crystal X-ray diffraction analysis, and asymmetric catalysis.

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