A near-infrared phosphorescent probe for F− based on a cationic iridium(III) complex with triarylboron moieties

In this work, a near-infrared (NIR) phosphorescent probe for F − based on a cationic Ir(III) complex [Ir(Bpq) 2 (quqo)]PF 6 ( 1 ) with dimesitylboryl (Mes2B) groups on the cyclometalated C∧N ligands (Bpq) and 2-(quinolin-2-yl)quinoxaline (quqo) as N∧N ligand was designed and synthesized. The excited...

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Veröffentlicht in:Science China. Chemistry 2011-11, Vol.54 (11), p.1750-1758
Hauptverfasser: Xu, WenJuan, Liu, ShuJuan, Zhao, Qiang, Ma, TingChun, Sun, Shi, Zhao, XinYan, Huang, Wei
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container_end_page 1758
container_issue 11
container_start_page 1750
container_title Science China. Chemistry
container_volume 54
creator Xu, WenJuan
Liu, ShuJuan
Zhao, Qiang
Ma, TingChun
Sun, Shi
Zhao, XinYan
Huang, Wei
description In this work, a near-infrared (NIR) phosphorescent probe for F − based on a cationic Ir(III) complex [Ir(Bpq) 2 (quqo)]PF 6 ( 1 ) with dimesitylboryl (Mes2B) groups on the cyclometalated C∧N ligands (Bpq) and 2-(quinolin-2-yl)quinoxaline (quqo) as N∧N ligand was designed and synthesized. The excited state properties of 1 were investigated in detail using molecular orbital calculations and experimental methods. Upon excitation, complex 1 shows NIR phosphorescent emission around 680 nm. Interestingly, the complex can be excited with long wavelength around 610 nm. Such long-wavelength excitation can reduce the background emission interference and improve the signal-to-noise ratio. Furthermore, the selective binding between boron atom and F − can give rise to the quenching of emission and realize the near-infrared phosphorescent sensing for F − . We wish that the results reported herein will be helpful for the further design of excellent near-infrared phosphorescent probes based on heavy-metal complexes.
doi_str_mv 10.1007/s11426-011-4359-y
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Chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, WenJuan</au><au>Liu, ShuJuan</au><au>Zhao, Qiang</au><au>Ma, TingChun</au><au>Sun, Shi</au><au>Zhao, XinYan</au><au>Huang, Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A near-infrared phosphorescent probe for F− based on a cationic iridium(III) complex with triarylboron moieties</atitle><jtitle>Science China. Chemistry</jtitle><stitle>Sci. China Chem</stitle><date>2011-11-01</date><risdate>2011</risdate><volume>54</volume><issue>11</issue><spage>1750</spage><epage>1758</epage><pages>1750-1758</pages><issn>1674-7291</issn><eissn>1869-1870</eissn><abstract>In this work, a near-infrared (NIR) phosphorescent probe for F − based on a cationic Ir(III) complex [Ir(Bpq) 2 (quqo)]PF 6 ( 1 ) with dimesitylboryl (Mes2B) groups on the cyclometalated C∧N ligands (Bpq) and 2-(quinolin-2-yl)quinoxaline (quqo) as N∧N ligand was designed and synthesized. The excited state properties of 1 were investigated in detail using molecular orbital calculations and experimental methods. Upon excitation, complex 1 shows NIR phosphorescent emission around 680 nm. Interestingly, the complex can be excited with long wavelength around 610 nm. Such long-wavelength excitation can reduce the background emission interference and improve the signal-to-noise ratio. Furthermore, the selective binding between boron atom and F − can give rise to the quenching of emission and realize the near-infrared phosphorescent sensing for F − . We wish that the results reported herein will be helpful for the further design of excellent near-infrared phosphorescent probes based on heavy-metal complexes.</abstract><cop>Heidelberg</cop><pub>SP Science China Press</pub><doi>10.1007/s11426-011-4359-y</doi><tpages>9</tpages></addata></record>
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subjects Background noise
Cations
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Coordination compounds
Excitation
Iridium compounds
Ligands
Molecular orbitals
Near infrared radiation
Phosphorescence
Quinoxalines
Selective binding
Signal to noise ratio
title A near-infrared phosphorescent probe for F− based on a cationic iridium(III) complex with triarylboron moieties
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