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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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 |
work_keys_str_mv |
AT aqsahabib cnibondfunctionalizationinthereactionofbinuclearcyclometallatedniiicomplexeswithchlorophosphines AT sharonriaz cnibondfunctionalizationinthereactionofbinuclearcyclometallatedniiicomplexeswithchlorophosphines AT ishaqahmad cnibondfunctionalizationinthereactionofbinuclearcyclometallatedniiicomplexeswithchlorophosphines AT durenajafiqbal cnibondfunctionalizationinthereactionofbinuclearcyclometallatedniiicomplexeswithchlorophosphines AT shaguftakamal cnibondfunctionalizationinthereactionofbinuclearcyclometallatedniiicomplexeswithchlorophosphines |
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