{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["3(8)"],"submitter":["Sen P"],"pubmed_abstract":["A series of asymmetrically substituted free-base di- and tetra-phenylporphyrins and the associated Zn-phenylporphyrins were synthesized and studied by X-ray diffraction, NMR, infrared, electronic absorption spectra, as well as fluorescence emission spectroscopy, along with theoretical simulations of the electronic and vibration structures. The synthesis selectively afforded trans-A₂B₂ porphyrins, without scrambling observed, where the AA and BB were taken as donor- and acceptor-substituted phenyl groups. The combined results point to similar properties to symmetrically substituted porphyrins reported in the literature. The differences in FTIR and fluorescence were analyzed by means of detailed density functional theory (DFT) calculations. The X-ray diffraction analysis for single crystals "],"journal":["Materials (Basel, Switzerland)"],"pagination":["4446-4475"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5445833"],"repository":["biostudies-literature"],"pubmed_title":["Fluorescence and FTIR Spectra Analysis of Trans-A₂B₂-Substituted Di- and Tetra-Phenyl Porphyrins."],"pmcid":["PMC5445833"],"pubmed_authors":["Minaev B","Bretonniere Y","Baryshnikov G","Sen P","Duboisset J","Mohammed A","Agren H","Hirel C","Lee HH","Lindgren M","Minaeva V","Andraud C","Aronica C"],"additional_accession":[]},"is_claimable":false,"name":"Fluorescence and FTIR Spectra Analysis of Trans-A₂B₂-Substituted Di- and Tetra-Phenyl Porphyrins.","description":"A series of asymmetrically substituted free-base di- and tetra-phenylporphyrins and the associated Zn-phenylporphyrins were synthesized and studied by X-ray diffraction, NMR, infrared, electronic absorption spectra, as well as fluorescence emission spectroscopy, along with theoretical simulations of the electronic and vibration structures. The synthesis selectively afforded trans-A₂B₂ porphyrins, without scrambling observed, where the AA and BB were taken as donor- and acceptor-substituted phenyl groups. The combined results point to similar properties to symmetrically substituted porphyrins reported in the literature. The differences in FTIR and fluorescence were analyzed by means of detailed density functional theory (DFT) calculations. The X-ray diffraction analysis for single crystals ","dates":{"release":"2010-01-01T00:00:00Z","publication":"2010 Aug","modification":"2025-04-05T12:01:17.404Z","creation":"2019-03-27T02:46:05Z"},"accession":"S-EPMC5445833","cross_references":{"pubmed":["28883336"],"doi":["10.3390/ma3084446"]}}