Phosphorescent Cellular Probes and Uptake Indicators Derived from Cyclometalated Iridium(III) Bipyridine Complexes Appended with a Glucose or Galactose Entity

A series of phosphorescent cyclometalated iridium­(III) polypyridine complexes appended with a β-d-glucose moiety [Ir­(N∧C)2(bpy-TEG-ONCH3-β-d-glc)]­(PF6) [bpy-TEG-ONCH3-β-d-glc = 4-(10-N-methyl-N-(β-d-glucopyranosyl)-amino-oxy-2,5,8-trioxa-dec-1-yl)-4′-methyl-2,2′-bipyridine; HN∧C = 2-((1,1′-biphen...

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Veröffentlicht in:Inorganic chemistry 2013-11, Vol.52 (22), p.13029-13041
Hauptverfasser: Law, Wendell Ho-Tin, Lee, Lawrence Cho-Cheung, Louie, Man-Wai, Liu, Hua-Wei, Ang, Tim Wai-Hung, Lo, Kenneth Kam-Wing
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container_issue 22
container_start_page 13029
container_title Inorganic chemistry
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creator Law, Wendell Ho-Tin
Lee, Lawrence Cho-Cheung
Louie, Man-Wai
Liu, Hua-Wei
Ang, Tim Wai-Hung
Lo, Kenneth Kam-Wing
description A series of phosphorescent cyclometalated iridium­(III) polypyridine complexes appended with a β-d-glucose moiety [Ir­(N∧C)2(bpy-TEG-ONCH3-β-d-glc)]­(PF6) [bpy-TEG-ONCH3-β-d-glc = 4-(10-N-methyl-N-(β-d-glucopyranosyl)-amino-oxy-2,5,8-trioxa-dec-1-yl)-4′-methyl-2,2′-bipyridine; HN∧C = 2-((1,1′-biphenyl)-4-yl)­benzothiazole) (Hbt) (1a), 2-phenylpyridine (Hppy) (2a), 2-phenylquinoline (Hpq) (3a), 7,8-benzoquinoline (Hbzq) (4a)] has been synthesized and characterized. The d-galactose counterparts [Ir­(N∧C)2(bpy-TEG-ONCH3-β-d-gal)]­(PF6) [bpy-TEG-ONCH3-β-d-gal = 4-(10-N-methyl-N-(β-d-galactopyranosyl)-amino-oxy-2,5,8-trioxa-dec-1-yl)-4′-methyl-2,2′-bipyridine; HN∧C = Hbt (1b), Hppy (2b), Hpq (3b), Hbzq (4b)] and a sugar-free bt complex [Ir­(bt)2(bpy-TEG-OMe)]­(PF6) [bpy-TEG-OMe = 4-(2,5,8,11-tetraoxa-dodec-1-yl)-4′-methyl-2,2′-bipyridine] (1c) have also been prepared. Upon photoexcitation, all the complexes displayed intense and long-lived triplet metal-to-ligand charge-transfer (3MLCT) [dπ­(Ir) → π*­(N∧N)] or triplet intraligand (3IL) (π → π*) (N∧C and N∧N) emission. The lipophilicity, the cellular uptake efficiency, and cytotoxicity of the complexes toward human cervix epithelioid carcinoma cells (HeLa) have been examined. Temperature dependence and chemical inhibition experiments indicated that the transport of bt–glucose complex 1a across the cell membrane occurred through an energy-requiring process such as endocytosis, in additional to a pathway that was mediated by glucose transporters (GLUTs). Importantly, the cellular uptake efficiency of this complex was found to be strongly dependent on hormonal stimulation and inhibition, rendering it a new phosphorescent metabolic indicator. Additionally, laser-scanning confocal microscopy revealed that the complex was localized in the mitochondria and highly resistant to photobleaching compared to a fluorescent organic glucose derivative 2-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)­amino)-2-deoxy-d-glucose (2-NBDG).
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The d-galactose counterparts [Ir­(N∧C)2(bpy-TEG-ONCH3-β-d-gal)]­(PF6) [bpy-TEG-ONCH3-β-d-gal = 4-(10-N-methyl-N-(β-d-galactopyranosyl)-amino-oxy-2,5,8-trioxa-dec-1-yl)-4′-methyl-2,2′-bipyridine; HN∧C = Hbt (1b), Hppy (2b), Hpq (3b), Hbzq (4b)] and a sugar-free bt complex [Ir­(bt)2(bpy-TEG-OMe)]­(PF6) [bpy-TEG-OMe = 4-(2,5,8,11-tetraoxa-dodec-1-yl)-4′-methyl-2,2′-bipyridine] (1c) have also been prepared. Upon photoexcitation, all the complexes displayed intense and long-lived triplet metal-to-ligand charge-transfer (3MLCT) [dπ­(Ir) → π*­(N∧N)] or triplet intraligand (3IL) (π → π*) (N∧C and N∧N) emission. The lipophilicity, the cellular uptake efficiency, and cytotoxicity of the complexes toward human cervix epithelioid carcinoma cells (HeLa) have been examined. Temperature dependence and chemical inhibition experiments indicated that the transport of bt–glucose complex 1a across the cell membrane occurred through an energy-requiring process such as endocytosis, in additional to a pathway that was mediated by glucose transporters (GLUTs). Importantly, the cellular uptake efficiency of this complex was found to be strongly dependent on hormonal stimulation and inhibition, rendering it a new phosphorescent metabolic indicator. Additionally, laser-scanning confocal microscopy revealed that the complex was localized in the mitochondria and highly resistant to photobleaching compared to a fluorescent organic glucose derivative 2-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)­amino)-2-deoxy-d-glucose (2-NBDG).</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/ic401714p</identifier><identifier>PMID: 24191646</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>2,2'-Dipyridyl - analysis ; 2,2'-Dipyridyl - chemistry ; 2,2'-Dipyridyl - metabolism ; Biological Transport ; Coordination Complexes - analysis ; Coordination Complexes - chemistry ; Coordination Complexes - metabolism ; Endocytosis ; Galactose - analysis ; Galactose - chemistry ; Galactose - metabolism ; Glucose - analysis ; Glucose - chemistry ; Glucose - metabolism ; HeLa Cells ; Humans ; Iridium - analysis ; Iridium - chemistry ; Iridium - metabolism ; Luminescent Agents - analysis ; Luminescent Agents - chemistry ; Luminescent Agents - metabolism</subject><ispartof>Inorganic chemistry, 2013-11, Vol.52 (22), p.13029-13041</ispartof><rights>Copyright © 2013 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a315t-f8d24a99c491f89fdb309dad06e2c0ccbddcd1f76d30c4ebf37cdbd0542dcf203</citedby><cites>FETCH-LOGICAL-a315t-f8d24a99c491f89fdb309dad06e2c0ccbddcd1f76d30c4ebf37cdbd0542dcf203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ic401714p$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ic401714p$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24191646$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Law, Wendell Ho-Tin</creatorcontrib><creatorcontrib>Lee, Lawrence Cho-Cheung</creatorcontrib><creatorcontrib>Louie, Man-Wai</creatorcontrib><creatorcontrib>Liu, Hua-Wei</creatorcontrib><creatorcontrib>Ang, Tim Wai-Hung</creatorcontrib><creatorcontrib>Lo, Kenneth Kam-Wing</creatorcontrib><title>Phosphorescent Cellular Probes and Uptake Indicators Derived from Cyclometalated Iridium(III) Bipyridine Complexes Appended with a Glucose or Galactose Entity</title><title>Inorganic chemistry</title><addtitle>Inorg. Chem</addtitle><description>A series of phosphorescent cyclometalated iridium­(III) polypyridine complexes appended with a β-d-glucose moiety [Ir­(N∧C)2(bpy-TEG-ONCH3-β-d-glc)]­(PF6) [bpy-TEG-ONCH3-β-d-glc = 4-(10-N-methyl-N-(β-d-glucopyranosyl)-amino-oxy-2,5,8-trioxa-dec-1-yl)-4′-methyl-2,2′-bipyridine; HN∧C = 2-((1,1′-biphenyl)-4-yl)­benzothiazole) (Hbt) (1a), 2-phenylpyridine (Hppy) (2a), 2-phenylquinoline (Hpq) (3a), 7,8-benzoquinoline (Hbzq) (4a)] has been synthesized and characterized. The d-galactose counterparts [Ir­(N∧C)2(bpy-TEG-ONCH3-β-d-gal)]­(PF6) [bpy-TEG-ONCH3-β-d-gal = 4-(10-N-methyl-N-(β-d-galactopyranosyl)-amino-oxy-2,5,8-trioxa-dec-1-yl)-4′-methyl-2,2′-bipyridine; HN∧C = Hbt (1b), Hppy (2b), Hpq (3b), Hbzq (4b)] and a sugar-free bt complex [Ir­(bt)2(bpy-TEG-OMe)]­(PF6) [bpy-TEG-OMe = 4-(2,5,8,11-tetraoxa-dodec-1-yl)-4′-methyl-2,2′-bipyridine] (1c) have also been prepared. Upon photoexcitation, all the complexes displayed intense and long-lived triplet metal-to-ligand charge-transfer (3MLCT) [dπ­(Ir) → π*­(N∧N)] or triplet intraligand (3IL) (π → π*) (N∧C and N∧N) emission. The lipophilicity, the cellular uptake efficiency, and cytotoxicity of the complexes toward human cervix epithelioid carcinoma cells (HeLa) have been examined. Temperature dependence and chemical inhibition experiments indicated that the transport of bt–glucose complex 1a across the cell membrane occurred through an energy-requiring process such as endocytosis, in additional to a pathway that was mediated by glucose transporters (GLUTs). Importantly, the cellular uptake efficiency of this complex was found to be strongly dependent on hormonal stimulation and inhibition, rendering it a new phosphorescent metabolic indicator. Additionally, laser-scanning confocal microscopy revealed that the complex was localized in the mitochondria and highly resistant to photobleaching compared to a fluorescent organic glucose derivative 2-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)­amino)-2-deoxy-d-glucose (2-NBDG).</description><subject>2,2'-Dipyridyl - analysis</subject><subject>2,2'-Dipyridyl - chemistry</subject><subject>2,2'-Dipyridyl - metabolism</subject><subject>Biological Transport</subject><subject>Coordination Complexes - analysis</subject><subject>Coordination Complexes - chemistry</subject><subject>Coordination Complexes - metabolism</subject><subject>Endocytosis</subject><subject>Galactose - analysis</subject><subject>Galactose - chemistry</subject><subject>Galactose - metabolism</subject><subject>Glucose - analysis</subject><subject>Glucose - chemistry</subject><subject>Glucose - metabolism</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Iridium - analysis</subject><subject>Iridium - chemistry</subject><subject>Iridium - metabolism</subject><subject>Luminescent Agents - analysis</subject><subject>Luminescent Agents - chemistry</subject><subject>Luminescent Agents - metabolism</subject><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc9u1DAQhy0EokvhwAsgX5Daw8I4cbL1saRliVSJHqjELXLssdbFiY3tAPsyfVa82tITp_mjT580vyHkLYMPDCr20SoObMN4eEZWrKlg3TD4_pysAErP2lackFcp3QOAqHn7kpxUnAnW8nZFHm53PoWdj5gUzpl26NziZKS30Y-YqJw1vQtZ_kDaz9oqmX1M9Aqj_YWamugn2u2V8xNm6WQuuz5abZfprO_7c_rJhv1hnpF2fgoO_xTnZQg464L-tnlHJd26RfmE1Ee6LRKVD8P1nG3evyYvjHQJ3zzWU3L3-fpb92V983Xbd5c3a1mzJq_Nha64FEJxwcyFMHqsQWipocVKgVKj1kozs2l1DYrjaOqN0qOGhldamQrqU3J29Ibofy6Y8jDZEohzcka_pIHxRjRtyfqAnh9RFX1KEc0Qop1k3A8MhsM7hqd3FPbdo3YZJ9RP5L_8C_D-CEiVhnu_xLlc-R_RXwZ4lR0</recordid><startdate>20131118</startdate><enddate>20131118</enddate><creator>Law, Wendell Ho-Tin</creator><creator>Lee, Lawrence Cho-Cheung</creator><creator>Louie, Man-Wai</creator><creator>Liu, Hua-Wei</creator><creator>Ang, Tim Wai-Hung</creator><creator>Lo, Kenneth Kam-Wing</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20131118</creationdate><title>Phosphorescent Cellular Probes and Uptake Indicators Derived from Cyclometalated Iridium(III) Bipyridine Complexes Appended with a Glucose or Galactose Entity</title><author>Law, Wendell Ho-Tin ; Lee, Lawrence Cho-Cheung ; Louie, Man-Wai ; Liu, Hua-Wei ; Ang, Tim Wai-Hung ; Lo, Kenneth Kam-Wing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a315t-f8d24a99c491f89fdb309dad06e2c0ccbddcd1f76d30c4ebf37cdbd0542dcf203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>2,2'-Dipyridyl - analysis</topic><topic>2,2'-Dipyridyl - chemistry</topic><topic>2,2'-Dipyridyl - metabolism</topic><topic>Biological Transport</topic><topic>Coordination Complexes - analysis</topic><topic>Coordination Complexes - chemistry</topic><topic>Coordination Complexes - metabolism</topic><topic>Endocytosis</topic><topic>Galactose - analysis</topic><topic>Galactose - chemistry</topic><topic>Galactose - metabolism</topic><topic>Glucose - analysis</topic><topic>Glucose - chemistry</topic><topic>Glucose - metabolism</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Iridium - analysis</topic><topic>Iridium - chemistry</topic><topic>Iridium - metabolism</topic><topic>Luminescent Agents - analysis</topic><topic>Luminescent Agents - chemistry</topic><topic>Luminescent Agents - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Law, Wendell Ho-Tin</creatorcontrib><creatorcontrib>Lee, Lawrence Cho-Cheung</creatorcontrib><creatorcontrib>Louie, Man-Wai</creatorcontrib><creatorcontrib>Liu, Hua-Wei</creatorcontrib><creatorcontrib>Ang, Tim Wai-Hung</creatorcontrib><creatorcontrib>Lo, Kenneth Kam-Wing</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Law, Wendell Ho-Tin</au><au>Lee, Lawrence Cho-Cheung</au><au>Louie, Man-Wai</au><au>Liu, Hua-Wei</au><au>Ang, Tim Wai-Hung</au><au>Lo, Kenneth Kam-Wing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phosphorescent Cellular Probes and Uptake Indicators Derived from Cyclometalated Iridium(III) Bipyridine Complexes Appended with a Glucose or Galactose Entity</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2013-11-18</date><risdate>2013</risdate><volume>52</volume><issue>22</issue><spage>13029</spage><epage>13041</epage><pages>13029-13041</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>A series of phosphorescent cyclometalated iridium­(III) polypyridine complexes appended with a β-d-glucose moiety [Ir­(N∧C)2(bpy-TEG-ONCH3-β-d-glc)]­(PF6) [bpy-TEG-ONCH3-β-d-glc = 4-(10-N-methyl-N-(β-d-glucopyranosyl)-amino-oxy-2,5,8-trioxa-dec-1-yl)-4′-methyl-2,2′-bipyridine; HN∧C = 2-((1,1′-biphenyl)-4-yl)­benzothiazole) (Hbt) (1a), 2-phenylpyridine (Hppy) (2a), 2-phenylquinoline (Hpq) (3a), 7,8-benzoquinoline (Hbzq) (4a)] has been synthesized and characterized. The d-galactose counterparts [Ir­(N∧C)2(bpy-TEG-ONCH3-β-d-gal)]­(PF6) [bpy-TEG-ONCH3-β-d-gal = 4-(10-N-methyl-N-(β-d-galactopyranosyl)-amino-oxy-2,5,8-trioxa-dec-1-yl)-4′-methyl-2,2′-bipyridine; HN∧C = Hbt (1b), Hppy (2b), Hpq (3b), Hbzq (4b)] and a sugar-free bt complex [Ir­(bt)2(bpy-TEG-OMe)]­(PF6) [bpy-TEG-OMe = 4-(2,5,8,11-tetraoxa-dodec-1-yl)-4′-methyl-2,2′-bipyridine] (1c) have also been prepared. Upon photoexcitation, all the complexes displayed intense and long-lived triplet metal-to-ligand charge-transfer (3MLCT) [dπ­(Ir) → π*­(N∧N)] or triplet intraligand (3IL) (π → π*) (N∧C and N∧N) emission. The lipophilicity, the cellular uptake efficiency, and cytotoxicity of the complexes toward human cervix epithelioid carcinoma cells (HeLa) have been examined. Temperature dependence and chemical inhibition experiments indicated that the transport of bt–glucose complex 1a across the cell membrane occurred through an energy-requiring process such as endocytosis, in additional to a pathway that was mediated by glucose transporters (GLUTs). Importantly, the cellular uptake efficiency of this complex was found to be strongly dependent on hormonal stimulation and inhibition, rendering it a new phosphorescent metabolic indicator. Additionally, laser-scanning confocal microscopy revealed that the complex was localized in the mitochondria and highly resistant to photobleaching compared to a fluorescent organic glucose derivative 2-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)­amino)-2-deoxy-d-glucose (2-NBDG).</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>24191646</pmid><doi>10.1021/ic401714p</doi><tpages>13</tpages></addata></record>
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subjects 2,2'-Dipyridyl - analysis
2,2'-Dipyridyl - chemistry
2,2'-Dipyridyl - metabolism
Biological Transport
Coordination Complexes - analysis
Coordination Complexes - chemistry
Coordination Complexes - metabolism
Endocytosis
Galactose - analysis
Galactose - chemistry
Galactose - metabolism
Glucose - analysis
Glucose - chemistry
Glucose - metabolism
HeLa Cells
Humans
Iridium - analysis
Iridium - chemistry
Iridium - metabolism
Luminescent Agents - analysis
Luminescent Agents - chemistry
Luminescent Agents - metabolism
title Phosphorescent Cellular Probes and Uptake Indicators Derived from Cyclometalated Iridium(III) Bipyridine Complexes Appended with a Glucose or Galactose Entity
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