Synthesis and boron interaction of new amino acid containing phthalocyanines and the precursor
| dc.authorscopusid | 55198967300 | |
| dc.authorscopusid | 23105409900 | |
| dc.authorscopusid | 35279899900 | |
| dc.authorwosid | GÜL, Ahmet/B-9622-2013 | |
| dc.authorwosid | Erdoğmuş, Ali/V-7213-2019 | |
| dc.contributor.author | Baseren, Sukran Cenikli | |
| dc.contributor.author | Erdogmus, Ali | |
| dc.contributor.author | Gul, Ahmet | |
| dc.date.accessioned | 2024-05-25T11:19:30Z | |
| dc.date.available | 2024-05-25T11:19:30Z | |
| dc.date.issued | 2018 | |
| dc.department | Okan University | en_US |
| dc.department-temp | [Baseren, Sukran Cenikli; Gul, Ahmet] Istanbul Tech Univ, Dept Chem, TR-34469 Istanbul, Turkey; [Baseren, Sukran Cenikli] Okan Univ, Pathol Lab Tech Programme, Vocat Sch Hlth Serv, Istanbul, Turkey; [Erdogmus, Ali] Yildiz Tech Univ, Dept Chem, TR-34210 Istanbul, Turkey | en_US |
| dc.description.abstract | A new phthalonitrile precursor with tyrosine substituent and the zinc phthalocyanine derived from it were synthesized and their interaction with diphenylborinic acid was studied. The new compounds were characterized by using elemental analysis, IR, H-1 and B-11-NMR and UV-VIS spectral data. B-11-NMR data demonstrated that boron atom attached to the phthalonitrile precursor is in a bulky tetra-coordinated state with the formation of a coordinative N-B bond while completely planar phthalocyanine moieties with high aggregation tendencies at the concentrations used in NMR measurements lead the borinic ester side of the molecule into a planar tri-coordinated form. Moreover, the consequences of the presence of diphenylborinic ester groups on the spectral, photophysical and photochemical properties of the new zinc phthalocyanine are investigated in detail. (C) 2018 Elsevier B.V. All rights reserved. | en_US |
| dc.description.sponsorship | Research Fund of the Technical University of Istanbul; Turkish Academy of Sciences (TUBA) | en_US |
| dc.description.sponsorship | This work was supported by the Research Fund of the Technical University of Istanbul. AG thanks Turkish Academy of Sciences (TUBA) for partial support. | en_US |
| dc.identifier.citationcount | 6 | |
| dc.identifier.doi | 10.1016/j.jorganchem.2018.04.016 | |
| dc.identifier.endpage | 111 | en_US |
| dc.identifier.issn | 0022-328X | |
| dc.identifier.issn | 1872-8561 | |
| dc.identifier.scopus | 2-s2.0-85046015959 | |
| dc.identifier.scopusquality | Q3 | |
| dc.identifier.startpage | 105 | en_US |
| dc.identifier.uri | https://doi.org/10.1016/j.jorganchem.2018.04.016 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14517/424 | |
| dc.identifier.volume | 866 | en_US |
| dc.identifier.wos | WOS:000432600900013 | |
| dc.identifier.wosquality | Q2 | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Science Sa | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.scopus.citedbyCount | 7 | |
| dc.subject | Phthalocyanine | en_US |
| dc.subject | Diphenylborinic acid | en_US |
| dc.subject | Borinate complex | en_US |
| dc.subject | Photochemistry | en_US |
| dc.subject | Fluorescence | en_US |
| dc.title | Synthesis and boron interaction of new amino acid containing phthalocyanines and the precursor | en_US |
| dc.type | Article | en_US |
| dc.wos.citedbyCount | 7 |