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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9330
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dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:21Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:21Z-
dc.date.issued2014-
dc.identifier.citationRajakannu, P., Mobin, S. M., & Sathiyendiran, M. (2014). Thiophene/furan units decorated unsymmetrical dinuclear metallocalix[4]arenes. Journal of Organometallic Chemistry, 771, 68-77. doi:10.1016/j.jorganchem.2014.03.028en_US
dc.identifier.issn0022-328X-
dc.identifier.otherEID(2-s2.0-84908448338)-
dc.identifier.urihttps://doi.org/10.1016/j.jorganchem.2014.03.028-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9330-
dc.description.abstractTwelve new dinuclear metallocalix[4]arenes (1-12) decorated with two thiophene units/two furan units were synthesized using a newly designed flexible ditopic nitrogen donors, a bis-chelating ligands, and Re2(CO)10 and were structurally characterized by various spectroscopic methods. The structures of 1, 5 and 9 were confirmed by single crystal X-ray diffraction analysis. The photophysical properties of the ligands were studied. The structures of 1, 3 and 5-12 were optimized using DFT-calculations. © 2014 Elsevier B.V.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.sourceJournal of Organometallic Chemistryen_US
dc.subjectBenzimidazolesen_US
dc.subjectCalix[4]arenesen_US
dc.subjectMetallocavitanden_US
dc.subjectMetallomacrocyclesen_US
dc.subjectSupramoleculesen_US
dc.subjectRheniumen_US
dc.titleThiophene/furan units decorated unsymmetrical dinuclear metallocalix[4]arenesen_US
dc.typeJournal Articleen_US
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