Synthesis, characterization, crystal structure and predicting the second-order optical nonlinearity of a new dicobalt(III) complex with Schiff base ligand

Zarei, Seyed Amir; Piltan, Mohammad; Hassanzadeh, Keyumars; Akhtari, Keivan; Cinčić, Dominik

doi:10.1016/j.molstruc.2014.11.023

Cited by 18 publications

(9 citation statements)

References 49 publications

(37 reference statements)

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“…The photochromic and thermochromic properties of Schiff bases make their study interesting (Girisha et al, 2018). They form second-order NLO organic materials, which are being used in computers, optical communication and medical imaging (Zarei et al, 2015). Hydrazones also play an important role in curing diseases effectively with less toxicity.…”

Section: Chemical Contextmentioning

confidence: 99%

Crystal structure and Hirshfeld surface analysis of (E)-N′-benzylidene-4-chlorobenzenesulfonohydrazide and of its (E)-4-chloro-N′-(ortho- and para-methylbenzylidene)benzenesulfonohydrazide derivatives

2018

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The crystal structures of (E)-N′-(benzylidene)-4-chlorobenzenesulfonohydrazide (I) and its ortho- and para-methyl-substituted benzylidene derivatives, (E)-N′-(2-methylbenzylidene)-4-chloro-benzenesulfonohydrazide (II) and (E)-N′-(4-methylbenzylidene)-4-chlorobenzenesulfonohydrazide (III), have been studied to investigate the effect of substitution on the structural and supramolecular features of these compounds.

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Section: Chemical Contextmentioning

confidence: 99%

Crystal structure and Hirshfeld surface analysis of (E)-N′-benzylidene-4-chlorobenzenesulfonohydrazide and of its (E)-4-chloro-N′-(ortho- and para-methylbenzylidene)benzenesulfonohydrazide derivatives

2018

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“…Schiff base organic compounds are widely employed ligands in modern coordination chemistry because they are easily accessible and display high versatility (Zarei et al, 2015). Within this field, the coordination chemistry of H 2 salen [N,N 0bis(salicylidene)ethane-1,2-diamine] has been studied with virtually all transition metals.…”

Section: Chemical Contextmentioning

confidence: 99%

Packing polymorphism in the structure oftrans-aqua[N,N′-bis(salicylidene)ethane-1,2-diamine-κ⁴O,N,N′,O′]chloridomanganese(III) monohydrate

2018

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“…Schiff bazları fizyolojik ve farmakolojik özelliklerinden dolayı büyük önem taşımaktadır. Schiff bazları optik malzemeler, iletken polimerler ve boya yapımı gibi çeşitli endüstriyel proseslerde kullanılmaktadır (Zarei et al 2015). Bunun yanında antifungal, antibakteriyel, antikanser ve antiviral aktiviteler gibi çeşitli farmakolojik özelliklerede sahiptir (Dhahagani et al 2014).…”

Section: Introductionunclassified

Synthesis and Characterization of Schiff Base Derivatives Containing 2- Amino-1,3,4-Thiadiazole Ring

Tahtacı¹

2017

AKU-J. Sci. Eng.

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Anahtar kelimelerNitril türevleri; 2-Amino-1,3,4-tiyadiazol; Schiff bazı. ÖzetTiyadiazol ve schiff bazı içeren bileşikler heterosiklik kimyada önemli bir yere sahiptir. Bu bileşiklerin çeşitli biyolojik aktivite gösterdiği uzun yıllardır bilinmektedir. Schiff bazı ve bunların türevleri antienflammatuar, antidepresif, antibakteriyal özelliklerinin yanı sıra bazı türevlerinin herbisitlere ve fungisitlere karşıda etkin olduğu bilinmektedir. AbstractThe compounds with thiadiazole and schiff base have an important place in heterocyclic chemistry. It is known for many years that these compounds show biological activities. It is also known that Schiff base and their derivatives have antienflamatuar, antidepressive, and antibacterial features besides that some derivatives are effective against herbicides and fungicides. Due to these features, compounds including Schiff bases and derivatives are highly studied in current researches. In the light of these significant data we obtained through the literature review, the main purpose of this study is to synthesize and characterize the various substituent groups including both thiadiazole and schiff bases with potential biological activities. Therefore, beginning from various nitrile derivatives (1a-c) and 5-amino-1,3,4-thiadiazole-2-thiol (5), primarily 2-amino-1,3,4-thiadiazol derivatives (2a-c, 7a-c) have been synthesized. Then these compounds have been reacted with various aldehyde derivatives (3a-c) to synthesize schiff base derivatives (4a-i, 8a-i). The structures of the synthesized compounds were elucidated using IR, 1

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Synthesis, characterization, crystal structure and predicting the second-order optical nonlinearity of a new dicobalt(III) complex with Schiff base ligand

Cited by 18 publications

References 49 publications

Crystal structure and Hirshfeld surface analysis of (E)-N′-benzylidene-4-chlorobenzenesulfonohydrazide and of its (E)-4-chloro-N′-(ortho- and para-methylbenzylidene)benzenesulfonohydrazide derivatives

Crystal structure and Hirshfeld surface analysis of (E)-N′-benzylidene-4-chlorobenzenesulfonohydrazide and of its (E)-4-chloro-N′-(ortho- and para-methylbenzylidene)benzenesulfonohydrazide derivatives

Packing polymorphism in the structure oftrans-aqua[N,N′-bis(salicylidene)ethane-1,2-diamine-κ⁴O,N,N′,O′]chloridomanganese(III) monohydrate

Synthesis and Characterization of Schiff Base Derivatives Containing 2- Amino-1,3,4-Thiadiazole Ring

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Synthesis, characterization, crystal structure and predicting the second-order optical nonlinearity of a new dicobalt(III) complex with Schiff base ligand

Cited by 18 publications

References 49 publications

Crystal structure and Hirshfeld surface analysis of (E)-N′-benzylidene-4-chlorobenzenesulfonohydrazide and of its (E)-4-chloro-N′-(ortho- and para-methylbenzylidene)benzenesulfonohydrazide derivatives

Crystal structure and Hirshfeld surface analysis of (E)-N′-benzylidene-4-chlorobenzenesulfonohydrazide and of its (E)-4-chloro-N′-(ortho- and para-methylbenzylidene)benzenesulfonohydrazide derivatives

Packing polymorphism in the structure oftrans-aqua[N,N′-bis(salicylidene)ethane-1,2-diamine-κ4O,N,N′,O′]chloridomanganese(III) monohydrate

Synthesis and Characterization of Schiff Base Derivatives Containing 2- Amino-1,3,4-Thiadiazole Ring

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Packing polymorphism in the structure oftrans-aqua[N,N′-bis(salicylidene)ethane-1,2-diamine-κ⁴O,N,N′,O′]chloridomanganese(III) monohydrate