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DC Field | Value | Language |
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dc.contributor.author | Ladomenou, K. | en |
dc.contributor.author | Lazarides, T. | en |
dc.contributor.author | Panda, M. K. | en |
dc.contributor.author | Charalambidis, G. | en |
dc.contributor.author | Daphnomili, D. | en |
dc.contributor.author | Coutsolelos, A. G. | en |
dc.date.accessioned | 2015-11-24T16:41:31Z | - |
dc.date.available | 2015-11-24T16:41:31Z | - |
dc.identifier.issn | 0020-1669 | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/8431 | - |
dc.rights | Default Licence | - |
dc.subject | sensitized solar-cells | en |
dc.subject | cross-coupling reactions | en |
dc.subject | photoinduced electron-transfer | en |
dc.subject | substituted porphyrins | en |
dc.subject | efficient synthesis | en |
dc.subject | crystal-structures | en |
dc.subject | chiral porphyrins | en |
dc.subject | zinc porphyrin | en |
dc.subject | functionalized porphyrins | en |
dc.subject | self-organization | en |
dc.title | Meso-substituted Porphyrin Derivatives via Palladium-Catalyzed Amination Showing Wide Range Visible Absorption: Synthesis and Photophysical Studies | en |
heal.type | journalArticle | - |
heal.type.en | Journal article | en |
heal.type.el | Άρθρο Περιοδικού | el |
heal.identifier.primary | Doi 10.1021/Ic300714n | - |
heal.identifier.secondary | <Go to ISI>://000309739100012 | - |
heal.identifier.secondary | http://pubs.acs.org/doi/pdfplus/10.1021/ic300714n | - |
heal.language | en | - |
heal.access | campus | - |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
heal.publicationDate | 2012 | - |
heal.abstract | In recent years, there has been a growing interest in the design and synthesis of chromophores, which absorb in a wide region of the visible spectrum, as these constitute promising candidates for use as sensitizers in various solar energy conversion schemes. In this work, a palladium-catalyzed coupling reaction was employed in the synthesis of molecular triads in which two porphyrin or boron dipyrrin (BDP) chromophores are linked to the meso positions of a central Zn porphyrin (PZn) ring via an amino group. In the resulting conjugates, which strongly absorb over most of the visible region, the electronic properties of the constituent chromophores are largely retained while detailed emission experiments reveal the energy transfer pathways that occur in each triad. | en |
heal.publisher | American Chemical Society | en |
heal.journalName | Inorg Chem | en |
heal.journalType | peer reviewed | - |
heal.fullTextAvailability | TRUE | - |
Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ |
Files in This Item:
File | Description | Size | Format | |
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Ladomenou-2012-Meso-substituted Por.pdf | 580.94 kB | Adobe PDF | View/Open Request a copy |
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