Synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (II) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligands

Various azomethine-zinc(II) complexes (3a-c) of bis(salicylidene)cyclohexyl-1,2-diamino organic ligands were synthesized by one pot reaction of salicylaldehydes/2-hydroxy-1-naphthaldehyde (2 eq), cyclohexyl-1,2-diamine (1 eq) and zinc acetate (1 eq) in methanol solvent at reflux temperature. The syn...

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Main Authors: M. Srinivas, G.R. Vijayakumar, K.M. Mahadevan, H. Nagabhushana, H.S. Bhojya Naik
Format: Article
Language:English
Published: Elsevier 2017-06-01
Series:Journal of Science: Advanced Materials and Devices
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2468217916302337
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spelling doaj-b7aef3c8594a4c38860c137a1117c63d2020-11-24T22:48:07ZengElsevierJournal of Science: Advanced Materials and Devices2468-21792017-06-012215616410.1016/j.jsamd.2017.02.008Synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (II) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligandsM. Srinivas0G.R. Vijayakumar1K.M. Mahadevan2H. Nagabhushana3H.S. Bhojya Naik4Department of Chemistry, Kuvempu University, P. G. Centre, Kadur 577548, IndiaDepartment of Chemistry, University College of Science, Tumkur University, Tumakuru 572 103, IndiaDepartment of Chemistry, Kuvempu University, P. G. Centre, Kadur 577548, IndiaProf. C.N.R Rao Centre for Advanced Materials Research, Tumkur University, Tumkur 572 103, IndiaDepartment of Studies and Research in Industrial Chemistry, Kuvempu University, Jnana Sahyadri, Shankaraghatta 577 451, IndiaVarious azomethine-zinc(II) complexes (3a-c) of bis(salicylidene)cyclohexyl-1,2-diamino organic ligands were synthesized by one pot reaction of salicylaldehydes/2-hydroxy-1-naphthaldehyde (2 eq), cyclohexyl-1,2-diamine (1 eq) and zinc acetate (1 eq) in methanol solvent at reflux temperature. The synthesized complexes were characterized by FTIR, 1H NMR, and SEM. Their photophysical properties such as Photoluminescence (PL) and Diffused Reflectance Spectra (DRS) were studied. PL studies revealed that the emission peaks of the complexes in both solution and solid states appeared to occur at 395–600 nm and emitted blue light. The band gap energies determined from DRS were 2.98 eV (3a), 2.91 eV (3b), and 2.73 eV (3c). Based on these results, we ascertain that these Zn(II) complexes can serve as a suitable non-dopant blue light emitting compound for flat panel display applications. Latent fingerprint detection study indicated that the powder compounds show good adhesion and finger ridge details without background staining. The demonstrated method can be applied to detect fingerprints on all types of smooth surfaces.http://www.sciencedirect.com/science/article/pii/S2468217916302337Azomethine-zinc (II) complexesPhotoluminescenceOLEDSalicylaldehyde2-Hydroxy-1-naphthaldehydeFingerprint
collection DOAJ
language English
format Article
sources DOAJ
author M. Srinivas
G.R. Vijayakumar
K.M. Mahadevan
H. Nagabhushana
H.S. Bhojya Naik
spellingShingle M. Srinivas
G.R. Vijayakumar
K.M. Mahadevan
H. Nagabhushana
H.S. Bhojya Naik
Synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (II) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligands
Journal of Science: Advanced Materials and Devices
Azomethine-zinc (II) complexes
Photoluminescence
OLED
Salicylaldehyde
2-Hydroxy-1-naphthaldehyde
Fingerprint
author_facet M. Srinivas
G.R. Vijayakumar
K.M. Mahadevan
H. Nagabhushana
H.S. Bhojya Naik
author_sort M. Srinivas
title Synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (II) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligands
title_short Synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (II) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligands
title_full Synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (II) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligands
title_fullStr Synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (II) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligands
title_full_unstemmed Synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (II) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligands
title_sort synthesis, photoluminescence and forensic applications of blue light emitting azomethine-zinc (ii) complexes of bis(salicylidene)cyclohexyl-1,2-diamino based organic ligands
publisher Elsevier
series Journal of Science: Advanced Materials and Devices
issn 2468-2179
publishDate 2017-06-01
description Various azomethine-zinc(II) complexes (3a-c) of bis(salicylidene)cyclohexyl-1,2-diamino organic ligands were synthesized by one pot reaction of salicylaldehydes/2-hydroxy-1-naphthaldehyde (2 eq), cyclohexyl-1,2-diamine (1 eq) and zinc acetate (1 eq) in methanol solvent at reflux temperature. The synthesized complexes were characterized by FTIR, 1H NMR, and SEM. Their photophysical properties such as Photoluminescence (PL) and Diffused Reflectance Spectra (DRS) were studied. PL studies revealed that the emission peaks of the complexes in both solution and solid states appeared to occur at 395–600 nm and emitted blue light. The band gap energies determined from DRS were 2.98 eV (3a), 2.91 eV (3b), and 2.73 eV (3c). Based on these results, we ascertain that these Zn(II) complexes can serve as a suitable non-dopant blue light emitting compound for flat panel display applications. Latent fingerprint detection study indicated that the powder compounds show good adhesion and finger ridge details without background staining. The demonstrated method can be applied to detect fingerprints on all types of smooth surfaces.
topic Azomethine-zinc (II) complexes
Photoluminescence
OLED
Salicylaldehyde
2-Hydroxy-1-naphthaldehyde
Fingerprint
url http://www.sciencedirect.com/science/article/pii/S2468217916302337
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