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research article

New Cu (I) complexes as catalyst for "click" reaction: An experimental and computational study

Gholivand, Khodayar
•
Faraghi, Mohammad
•
Malekshah, Rahime Eshagi
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January 18, 2023
Applied Organometallic Chemistry

In this work, two novel well-defined Cu (I) complexes of a Schiff base ligand are described. For this purpose, N, N '-bis (trans-cinnamaldehyde) ethylenediimine [C20H20N2] (L) and Cu (I) complex of the type [CuC20H20N2)PPh3Cl] (C1) and [Cu(C20H20N2)PPh3Br] (C2) were synthesised. IR, NMR, XRD and TGA analyses were used to characterise these compounds and single-crystal X-ray crystallography confirmed the structure of the compounds. The catalytic activity of the synthesised complexes was studied in azide-alkyne click reaction (AAC) and the best reaction condition was 15 mol% catalyst, 30 min and 45 degrees C in water, which can be considered moderate catalytic activity for the complexes. Material Studio 2017 software was used to obtain the geometry, energy, HOMO and LUMO of all structures by the quantum calculations (module DMol(3) and LDA/PWC). The computational results showed catalyst C2 has more reactivity than catalyst C1, and the C1-catalysed products form faster than the C2-catalysed products exceptions 4a and 4b. Product 4b (resulting catalyst C2) is formed faster than product (4a).

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Type
research article
DOI
10.1002/aoc.6924
Web of Science ID

WOS:000914767100001

Author(s)
Gholivand, Khodayar
Faraghi, Mohammad
Malekshah, Rahime Eshagi
Jafari, Mohammadreza
Akbarzadeh, Ali Reza
Latifi, Reza
Fadaei-Tirani, Farzaneh  
Fallah, Nasrin
Farshadfar, Kaveh
Date Issued

2023-01-18

Publisher

WILEY

Published in
Applied Organometallic Chemistry
Volume

37

Issue

3

Article Number

e6924

Subjects

Chemistry, Applied

•

Chemistry, Inorganic & Nuclear

•

Chemistry

•

catalytic activity

•

click reaction

•

cu (i) complex

•

quantum calculations

•

schiff-bases

•

1,4-disubstituted 1,2,3-triazoles

•

recyclable catalyst

•

copper

•

chemistry

•

efficient

•

cycloaddition

•

green

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
ISIC-GE  
Available on Infoscience
February 13, 2023
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/194827
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