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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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_35519949</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2189502474</sourcerecordid><originalsourceid>FETCH-LOGICAL-c538t-bc971a83081099116dcde78d52aeb2606c265b77c5f3382f0594da12845e81753</originalsourceid><addsrcrecordid>eNpdkd1LwzAUxYMoOtQX35WBL1OI5qNJkxdhG37BUBB9Dml6WyNdO5NW2H9vdTo_7su9cH4czuUgdEDJGSVcnzsdLCFM0WwDDRhJJGZE6s1f9w7aj_GF9CMFZZJuox0uBNU60QM0nlQdYJj7tvV1ObQu-NzXgFtblpAPo6_eIIxOcOYjvsPP0EJo3NJV3g2dDRnUsIe2CltF2P_au-jp6vJxeoNn99e30_EMO8FVizOnU2oVJ4oSrSmVucshVblgFjImiXRMiixNnSg4V6wgQie5pUwlAhRNBd9FFyvfRZfNIXdQt8FWZhH83Ialaaw3f5XaP5uyeTOaSMoF6Q1GXwahee0gtmbuo4OqsjU0XTRMSkr6gEL16PE_9KXpQt2_ZxhVWhCWpElPna4oF5oYAxTrMJSYj3LMVD-MP8uZ9PDR7_hr9LuKHjhcASG6tfrTLn8HMy-SEg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2189502474</pqid></control><display><type>article</type><title>Blue-emitting acridine-tagged silver()-bis-N-heterocyclic carbene</title><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Prabusankar, Ganesan ; Muthukumaran, Nirmala ; Vaddamanu, Moulali ; Raju, Gembali ; Velappan, Kavitha ; Sathyanarayana, Arruri ; Masaya, Yamane ; Sugiyama, Shohei ; Hisano, Kyohei ; Tsutsumi, Osamu</creator><creatorcontrib>Prabusankar, Ganesan ; Muthukumaran, Nirmala ; Vaddamanu, Moulali ; Raju, Gembali ; Velappan, Kavitha ; Sathyanarayana, Arruri ; Masaya, Yamane ; Sugiyama, Shohei ; Hisano, Kyohei ; Tsutsumi, Osamu</creatorcontrib><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.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c9ra00281b</identifier><identifier>PMID: 35519949</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>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</subject><ispartof>RSC advances, 2019-01, Vol.9 (13), p.7543-755</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2019</rights><rights>This journal is © The Royal Society of Chemistry 2019 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c538t-bc971a83081099116dcde78d52aeb2606c265b77c5f3382f0594da12845e81753</citedby><cites>FETCH-LOGICAL-c538t-bc971a83081099116dcde78d52aeb2606c265b77c5f3382f0594da12845e81753</cites><orcidid>0000-0003-1772-135X ; 0000-0001-7506-9908</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061350/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061350/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35519949$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Prabusankar, Ganesan</creatorcontrib><creatorcontrib>Muthukumaran, Nirmala</creatorcontrib><creatorcontrib>Vaddamanu, Moulali</creatorcontrib><creatorcontrib>Raju, Gembali</creatorcontrib><creatorcontrib>Velappan, Kavitha</creatorcontrib><creatorcontrib>Sathyanarayana, Arruri</creatorcontrib><creatorcontrib>Masaya, Yamane</creatorcontrib><creatorcontrib>Sugiyama, Shohei</creatorcontrib><creatorcontrib>Hisano, Kyohei</creatorcontrib><creatorcontrib>Tsutsumi, Osamu</creatorcontrib><title>Blue-emitting acridine-tagged silver()-bis-N-heterocyclic carbene</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><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.</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 ; Muthukumaran, Nirmala ; Vaddamanu, Moulali ; Raju, Gembali ; Velappan, Kavitha ; Sathyanarayana, Arruri ; Masaya, Yamane ; Sugiyama, Shohei ; Hisano, Kyohei ; Tsutsumi, Osamu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c538t-bc971a83081099116dcde78d52aeb2606c265b77c5f3382f0594da12845e81753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Carbon 13</topic><topic>Cations</topic><topic>Chemical analysis</topic><topic>Chemistry</topic><topic>Crystal structure</topic><topic>Crystallography</topic><topic>Crystals</topic><topic>Fluorescence</topic><topic>Ligands</topic><topic>Molecular orbitals</topic><topic>Molecular structure</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Silver</topic><topic>Single crystals</topic><topic>Synthesis</topic><topic>Time correlation functions</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prabusankar, Ganesan</creatorcontrib><creatorcontrib>Muthukumaran, Nirmala</creatorcontrib><creatorcontrib>Vaddamanu, Moulali</creatorcontrib><creatorcontrib>Raju, Gembali</creatorcontrib><creatorcontrib>Velappan, Kavitha</creatorcontrib><creatorcontrib>Sathyanarayana, Arruri</creatorcontrib><creatorcontrib>Masaya, Yamane</creatorcontrib><creatorcontrib>Sugiyama, Shohei</creatorcontrib><creatorcontrib>Hisano, Kyohei</creatorcontrib><creatorcontrib>Tsutsumi, Osamu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prabusankar, Ganesan</au><au>Muthukumaran, Nirmala</au><au>Vaddamanu, Moulali</au><au>Raju, Gembali</au><au>Velappan, Kavitha</au><au>Sathyanarayana, Arruri</au><au>Masaya, Yamane</au><au>Sugiyama, Shohei</au><au>Hisano, Kyohei</au><au>Tsutsumi, Osamu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blue-emitting acridine-tagged silver()-bis-N-heterocyclic carbene</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>9</volume><issue>13</issue><spage>7543</spage><epage>755</epage><pages>7543-755</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>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.</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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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access |
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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