Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C4h octaarylphthalocyanines
Mulholland, Katie D. and Yoon, Sangbin and Rennie, Christopher C. and Sitch, Eleanor K. and McKay, Alasdair I. and Edkins, Katharina and Edkins, Robert M. (2020) Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C4h octaarylphthalocyanines. Chemical Communications, 56 (60). pp. 8452-8455. ISSN 1359-7345 (https://doi.org/10.1039/D0CC03161E)
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Abstract
Ir-catalysed borylation of phthalonitrile produces both 4-(Bpin)phthalonitrile (1) and 3,5-bis(Bpin)phthalonitrile (2), which are potential divergent intermediates for the synthesis of functionalized phthalocyanines. To exemplify the utility of 2, we have prepared a series of 3,5-bis-arylphthalonitriles that in turn undergo sterically controlled regioselective cyclotetramization to give previously unknown C4h 1,3,8,10,15,17,22,24-octaarylphthalocyanines.
ORCID iDs
Mulholland, Katie D., Yoon, Sangbin, Rennie, Christopher C., Sitch, Eleanor K., McKay, Alasdair I., Edkins, Katharina ORCID: https://orcid.org/0000-0002-6885-5457 and Edkins, Robert M. ORCID: https://orcid.org/0000-0001-6117-5275;-
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Item type: Article ID code: 72820 Dates: DateEvent4 August 2020Published18 June 2020Published Online18 June 2020Accepted17 March 2020SubmittedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry
Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical SciencesDepositing user: Pure Administrator Date deposited: 18 Jun 2020 13:40 Last modified: 21 Dec 2024 01:21 URI: https://strathprints.strath.ac.uk/id/eprint/72820