C-Ni bond functionalization in the reaction of binuclear cyclometallated Ni(II) complexes with chlorophosphines

This manuscript reports successful C-H nickellation of the aryl phosphinites (i-Pr2P(O-aryl) derived from un-substituted/substituted phenols: C6H5OH, 4-R-C6H4OH (R = F, MeO). Nickellation was observed with the phosphinites at an ortho-C-H position to generate Br-bridged dimers [{κP,κC-(i-Pr)2PO-aryl...

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Main Authors: Aqsa Habib, Sharon Riaz, Ishaq Ahmad, Dure Najaf Iqbal, Shagufta Kamal
Format: Article
Language:English
Published: Elsevier 2021-02-01
Series:Journal of Saudi Chemical Society
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1319610320301678
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spelling doaj-adf83e82b03e4d68bcdc60620faf0ebd2021-02-05T15:30:27ZengElsevierJournal of Saudi Chemical Society1319-61032021-02-01252101178C-Ni bond functionalization in the reaction of binuclear cyclometallated Ni(II) complexes with chlorophosphinesAqsa Habib0Sharon Riaz1Ishaq Ahmad2Dure Najaf Iqbal3Shagufta Kamal4Department of Chemistry, University of Sialkot, Sialkot, Punjab 51040, Pakistan; Corresponding author.Department of Chemistry, University of Sialkot, Sialkot, Punjab 51040, PakistanInstitute of Textiles and Clothing, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong KongDepartment of Chemistry, University of Lahore, Lahore, Punjab, PakistanDepartment of Biochemistry, Government College University, Faisalabad, Punjab 38040, PakistanThis manuscript reports successful C-H nickellation of the aryl phosphinites (i-Pr2P(O-aryl) derived from un-substituted/substituted phenols: C6H5OH, 4-R-C6H4OH (R = F, MeO). Nickellation was observed with the phosphinites at an ortho-C-H position to generate Br-bridged dimers [{κP,κC-(i-Pr)2PO-aryl}cNi(μ-Br)]2 (C1-C3). While conversion of monomeric complexes from dimeric cyclonickellated complexes, functionalization behaviour was studied under inert atmosphere by reacting synthesized complexes with R2PX in various solvents. In order to understand the feasibility of the reaction and to evaluate the properties of product of insertion, phosphinite-phosphine nickel complexes were also approached from a second side. Appearance of specific signals in NMR spectra of products, provided strong evidences of formation of the target products exhibiting fluxional behaviour.http://www.sciencedirect.com/science/article/pii/S1319610320301678FunctionalizationInsertionCyclonickellationPhosphinites
collection DOAJ
language English
format Article
sources DOAJ
author Aqsa Habib
Sharon Riaz
Ishaq Ahmad
Dure Najaf Iqbal
Shagufta Kamal
spellingShingle Aqsa Habib
Sharon Riaz
Ishaq Ahmad
Dure Najaf Iqbal
Shagufta Kamal
C-Ni bond functionalization in the reaction of binuclear cyclometallated Ni(II) complexes with chlorophosphines
Journal of Saudi Chemical Society
Functionalization
Insertion
Cyclonickellation
Phosphinites
author_facet Aqsa Habib
Sharon Riaz
Ishaq Ahmad
Dure Najaf Iqbal
Shagufta Kamal
author_sort Aqsa Habib
title C-Ni bond functionalization in the reaction of binuclear cyclometallated Ni(II) complexes with chlorophosphines
title_short C-Ni bond functionalization in the reaction of binuclear cyclometallated Ni(II) complexes with chlorophosphines
title_full C-Ni bond functionalization in the reaction of binuclear cyclometallated Ni(II) complexes with chlorophosphines
title_fullStr C-Ni bond functionalization in the reaction of binuclear cyclometallated Ni(II) complexes with chlorophosphines
title_full_unstemmed C-Ni bond functionalization in the reaction of binuclear cyclometallated Ni(II) complexes with chlorophosphines
title_sort c-ni bond functionalization in the reaction of binuclear cyclometallated ni(ii) complexes with chlorophosphines
publisher Elsevier
series Journal of Saudi Chemical Society
issn 1319-6103
publishDate 2021-02-01
description This manuscript reports successful C-H nickellation of the aryl phosphinites (i-Pr2P(O-aryl) derived from un-substituted/substituted phenols: C6H5OH, 4-R-C6H4OH (R = F, MeO). Nickellation was observed with the phosphinites at an ortho-C-H position to generate Br-bridged dimers [{κP,κC-(i-Pr)2PO-aryl}cNi(μ-Br)]2 (C1-C3). While conversion of monomeric complexes from dimeric cyclonickellated complexes, functionalization behaviour was studied under inert atmosphere by reacting synthesized complexes with R2PX in various solvents. In order to understand the feasibility of the reaction and to evaluate the properties of product of insertion, phosphinite-phosphine nickel complexes were also approached from a second side. Appearance of specific signals in NMR spectra of products, provided strong evidences of formation of the target products exhibiting fluxional behaviour.
topic Functionalization
Insertion
Cyclonickellation
Phosphinites
url http://www.sciencedirect.com/science/article/pii/S1319610320301678
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