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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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). |
doi_str_mv | 10.1021/ic401714p |
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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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