Blue-emitting acridine-tagged silver()-bis-N-heterocyclic carbene

Herein, the photophysical properties of an acridine derivative of a bis-N-heterocyclic carbene silver complex were investigated. The HOMO and LUMO energy differences between 9-[( N -methyl imidazol-2-ylidene)]acridine and 4,5-bis[( N -methyl-imidazol-2-ylidene)methyl]acridine were theoretically comp...

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Veröffentlicht in:RSC advances 2019-01, Vol.9 (13), p.7543-755
Hauptverfasser: Prabusankar, Ganesan, Muthukumaran, Nirmala, Vaddamanu, Moulali, Raju, Gembali, Velappan, Kavitha, Sathyanarayana, Arruri, Masaya, Yamane, Sugiyama, Shohei, Hisano, Kyohei, Tsutsumi, Osamu
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container_issue 13
container_start_page 7543
container_title RSC advances
container_volume 9
creator Prabusankar, Ganesan
Muthukumaran, Nirmala
Vaddamanu, Moulali
Raju, Gembali
Velappan, Kavitha
Sathyanarayana, Arruri
Masaya, Yamane
Sugiyama, Shohei
Hisano, Kyohei
Tsutsumi, Osamu
description Herein, the photophysical properties of an acridine derivative of a bis-N-heterocyclic carbene silver complex were investigated. The HOMO and LUMO energy differences between 9-[( N -methyl imidazol-2-ylidene)]acridine and 4,5-bis[( N -methyl-imidazol-2-ylidene)methyl]acridine were theoretically compared. Based on the calculation, the 4,5-bis N-heterocyclic carbene-tethered acridine type of ligand was found to be a potential source for tuning the fluorescent nature of the resultant metal derivatives. Thus, a 4,5-bis N-heterocyclic carbene (NHC)-tethered acridine silver( i ) salt was synthesized, and its photophysical properties were investigated. The 4,5-bis[( N -isopropylimidazol-2-ylidene)methyl]acridine silver( i ) hexafluorophosphate complex was obtained from the reaction between [4,5-bis{( N -isopropylimidazolium)methyl}acridine] hexafluorophosphate and Ag 2 O in very good yield; this molecule was characterized by elemental analysis and FTIR, multinuclear ( 1 H and 13 C) NMR, UV-Vis, and fluorescence spectroscopic techniques. The molecular structure has been confirmed by single-crystal X-ray diffraction analysis, which has revealed that the complex is a homoleptic mononuclear silver( i ) cationic solid. The charge of the Ag( i )-NHC cation is balanced by the hexafluorophosphate anion. The cationic moieties are closely packed in the chair and inverted chair forms where silver( i ) possesses a quasi-linear geometry. Moreover, the silver complex provided blue emission from all the three excitations with good fluorescence quantum yield. The fluorescence lifetime of the silver( i ) complex has been determined using the time-correlated single photon counting technique. Interestingly, the fluorescence decay pattern and the fluorescence lifetimes of the silver complex are largely different from those of the parent ligand acridine imidazolium salt. Moreover, the theoretical predictions have been found to be in good agreement with the experimental results. The synthesis and photophysical properties of blue-emitting acridine-tagged silver( i )-bis-N-heterocyclic carbene are reported.
doi_str_mv 10.1039/c9ra00281b
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The HOMO and LUMO energy differences between 9-[( N -methyl imidazol-2-ylidene)]acridine and 4,5-bis[( N -methyl-imidazol-2-ylidene)methyl]acridine were theoretically compared. Based on the calculation, the 4,5-bis N-heterocyclic carbene-tethered acridine type of ligand was found to be a potential source for tuning the fluorescent nature of the resultant metal derivatives. Thus, a 4,5-bis N-heterocyclic carbene (NHC)-tethered acridine silver( i ) salt was synthesized, and its photophysical properties were investigated. The 4,5-bis[( N -isopropylimidazol-2-ylidene)methyl]acridine silver( i ) hexafluorophosphate complex was obtained from the reaction between [4,5-bis{( N -isopropylimidazolium)methyl}acridine] hexafluorophosphate and Ag 2 O in very good yield; this molecule was characterized by elemental analysis and FTIR, multinuclear ( 1 H and 13 C) NMR, UV-Vis, and fluorescence spectroscopic techniques. The molecular structure has been confirmed by single-crystal X-ray diffraction analysis, which has revealed that the complex is a homoleptic mononuclear silver( i ) cationic solid. The charge of the Ag( i )-NHC cation is balanced by the hexafluorophosphate anion. The cationic moieties are closely packed in the chair and inverted chair forms where silver( i ) possesses a quasi-linear geometry. Moreover, the silver complex provided blue emission from all the three excitations with good fluorescence quantum yield. The fluorescence lifetime of the silver( i ) complex has been determined using the time-correlated single photon counting technique. Interestingly, the fluorescence decay pattern and the fluorescence lifetimes of the silver complex are largely different from those of the parent ligand acridine imidazolium salt. Moreover, the theoretical predictions have been found to be in good agreement with the experimental results. 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The HOMO and LUMO energy differences between 9-[( N -methyl imidazol-2-ylidene)]acridine and 4,5-bis[( N -methyl-imidazol-2-ylidene)methyl]acridine were theoretically compared. Based on the calculation, the 4,5-bis N-heterocyclic carbene-tethered acridine type of ligand was found to be a potential source for tuning the fluorescent nature of the resultant metal derivatives. Thus, a 4,5-bis N-heterocyclic carbene (NHC)-tethered acridine silver( i ) salt was synthesized, and its photophysical properties were investigated. The 4,5-bis[( N -isopropylimidazol-2-ylidene)methyl]acridine silver( i ) hexafluorophosphate complex was obtained from the reaction between [4,5-bis{( N -isopropylimidazolium)methyl}acridine] hexafluorophosphate and Ag 2 O in very good yield; this molecule was characterized by elemental analysis and FTIR, multinuclear ( 1 H and 13 C) NMR, UV-Vis, and fluorescence spectroscopic techniques. The molecular structure has been confirmed by single-crystal X-ray diffraction analysis, which has revealed that the complex is a homoleptic mononuclear silver( i ) cationic solid. The charge of the Ag( i )-NHC cation is balanced by the hexafluorophosphate anion. The cationic moieties are closely packed in the chair and inverted chair forms where silver( i ) possesses a quasi-linear geometry. Moreover, the silver complex provided blue emission from all the three excitations with good fluorescence quantum yield. The fluorescence lifetime of the silver( i ) complex has been determined using the time-correlated single photon counting technique. Interestingly, the fluorescence decay pattern and the fluorescence lifetimes of the silver complex are largely different from those of the parent ligand acridine imidazolium salt. Moreover, the theoretical predictions have been found to be in good agreement with the experimental results. The synthesis and photophysical properties of blue-emitting acridine-tagged silver( i )-bis-N-heterocyclic carbene are reported.</description><subject>Carbon 13</subject><subject>Cations</subject><subject>Chemical analysis</subject><subject>Chemistry</subject><subject>Crystal structure</subject><subject>Crystallography</subject><subject>Crystals</subject><subject>Fluorescence</subject><subject>Ligands</subject><subject>Molecular orbitals</subject><subject>Molecular structure</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Silver</subject><subject>Single crystals</subject><subject>Synthesis</subject><subject>Time correlation functions</subject><subject>X-ray diffraction</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpdkd1LwzAUxYMoOtQX35WBL1OI5qNJkxdhG37BUBB9Dml6WyNdO5NW2H9vdTo_7su9cH4czuUgdEDJGSVcnzsdLCFM0WwDDRhJJGZE6s1f9w7aj_GF9CMFZZJuox0uBNU60QM0nlQdYJj7tvV1ObQu-NzXgFtblpAPo6_eIIxOcOYjvsPP0EJo3NJV3g2dDRnUsIe2CltF2P_au-jp6vJxeoNn99e30_EMO8FVizOnU2oVJ4oSrSmVucshVblgFjImiXRMiixNnSg4V6wgQie5pUwlAhRNBd9FFyvfRZfNIXdQt8FWZhH83Ialaaw3f5XaP5uyeTOaSMoF6Q1GXwahee0gtmbuo4OqsjU0XTRMSkr6gEL16PE_9KXpQt2_ZxhVWhCWpElPna4oF5oYAxTrMJSYj3LMVD-MP8uZ9PDR7_hr9LuKHjhcASG6tfrTLn8HMy-SEg</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Prabusankar, Ganesan</creator><creator>Muthukumaran, Nirmala</creator><creator>Vaddamanu, Moulali</creator><creator>Raju, Gembali</creator><creator>Velappan, Kavitha</creator><creator>Sathyanarayana, Arruri</creator><creator>Masaya, Yamane</creator><creator>Sugiyama, Shohei</creator><creator>Hisano, Kyohei</creator><creator>Tsutsumi, Osamu</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1772-135X</orcidid><orcidid>https://orcid.org/0000-0001-7506-9908</orcidid></search><sort><creationdate>20190101</creationdate><title>Blue-emitting acridine-tagged silver()-bis-N-heterocyclic carbene</title><author>Prabusankar, Ganesan ; 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The HOMO and LUMO energy differences between 9-[( N -methyl imidazol-2-ylidene)]acridine and 4,5-bis[( N -methyl-imidazol-2-ylidene)methyl]acridine were theoretically compared. Based on the calculation, the 4,5-bis N-heterocyclic carbene-tethered acridine type of ligand was found to be a potential source for tuning the fluorescent nature of the resultant metal derivatives. Thus, a 4,5-bis N-heterocyclic carbene (NHC)-tethered acridine silver( i ) salt was synthesized, and its photophysical properties were investigated. The 4,5-bis[( N -isopropylimidazol-2-ylidene)methyl]acridine silver( i ) hexafluorophosphate complex was obtained from the reaction between [4,5-bis{( N -isopropylimidazolium)methyl}acridine] hexafluorophosphate and Ag 2 O in very good yield; this molecule was characterized by elemental analysis and FTIR, multinuclear ( 1 H and 13 C) NMR, UV-Vis, and fluorescence spectroscopic techniques. The molecular structure has been confirmed by single-crystal X-ray diffraction analysis, which has revealed that the complex is a homoleptic mononuclear silver( i ) cationic solid. The charge of the Ag( i )-NHC cation is balanced by the hexafluorophosphate anion. The cationic moieties are closely packed in the chair and inverted chair forms where silver( i ) possesses a quasi-linear geometry. Moreover, the silver complex provided blue emission from all the three excitations with good fluorescence quantum yield. The fluorescence lifetime of the silver( i ) complex has been determined using the time-correlated single photon counting technique. Interestingly, the fluorescence decay pattern and the fluorescence lifetimes of the silver complex are largely different from those of the parent ligand acridine imidazolium salt. Moreover, the theoretical predictions have been found to be in good agreement with the experimental results. The synthesis and photophysical properties of blue-emitting acridine-tagged silver( i )-bis-N-heterocyclic carbene are reported.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>35519949</pmid><doi>10.1039/c9ra00281b</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1772-135X</orcidid><orcidid>https://orcid.org/0000-0001-7506-9908</orcidid><oa>free_for_read</oa></addata></record>
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subjects Carbon 13
Cations
Chemical analysis
Chemistry
Crystal structure
Crystallography
Crystals
Fluorescence
Ligands
Molecular orbitals
Molecular structure
NMR
Nuclear magnetic resonance
Silver
Single crystals
Synthesis
Time correlation functions
X-ray diffraction
title Blue-emitting acridine-tagged silver()-bis-N-heterocyclic carbene
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