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Ultrafast Excited-State Dynamics in Vitamin B12 and Related Cob(III)alamins
Femtosecond transient IR and visible absorption spectroscopies have been employed to investigate the excited-state photophysics of vitamin B12 (cyanocobalamin, CNCbl) and the related cob(III)alamins, azidocobalamin (N3Cbl), and aquocobalamin (H2OCbl). Excitation of CNCbl, H2OCbl, or N3Cbl results in...
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Published in: | Journal of the American Chemical Society 2006-01, Vol.128 (3), p.801-808 |
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creator | Shiang, Joseph J Cole, Allwyn G Sension, Roseanne J Hang, Kun Weng, Yuxiang Trommel, Jenna S Marzilli, Luigi G Lian, Tianquan |
description | Femtosecond transient IR and visible absorption spectroscopies have been employed to investigate the excited-state photophysics of vitamin B12 (cyanocobalamin, CNCbl) and the related cob(III)alamins, azidocobalamin (N3Cbl), and aquocobalamin (H2OCbl). Excitation of CNCbl, H2OCbl, or N3Cbl results in rapid formation of a short-lived excited state followed by ground-state recovery on time scales ranging from a few picoseconds to a few tens of picoseconds. The lifetime of the intermediate state is influenced by the σ-donating ability of the axial ligand, decreasing in the order CNCbl > N3Cbl > H2OCbl, and by the polarity of the solvent, decreasing with increasing solvent polarity. The peak of the excited-state visible absorption spectrum is shifted to ca. 490 nm, and the shape of the spectrum is characteristic of weak axial ligands, similar to those observed for cob(II)alamin, base-off cobalamins, or cobinamides. Transient IR spectra of the upper CN and N3 ligands are red-shifted 20−30 cm-1 from the ground-state frequencies, consistent with a weakened Co−upper ligand bond. These results suggest that the transient intermediate state can be attributed to a corrin ring π to Co 3d z 2 ligand to metal charge transfer (LMCT) state. In this state bonds between the cobalt and the axial ligands are weakened and lengthened with respect to the corresponding ground states. |
doi_str_mv | 10.1021/ja054374+ |
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Excitation of CNCbl, H2OCbl, or N3Cbl results in rapid formation of a short-lived excited state followed by ground-state recovery on time scales ranging from a few picoseconds to a few tens of picoseconds. The lifetime of the intermediate state is influenced by the σ-donating ability of the axial ligand, decreasing in the order CNCbl > N3Cbl > H2OCbl, and by the polarity of the solvent, decreasing with increasing solvent polarity. The peak of the excited-state visible absorption spectrum is shifted to ca. 490 nm, and the shape of the spectrum is characteristic of weak axial ligands, similar to those observed for cob(II)alamin, base-off cobalamins, or cobinamides. Transient IR spectra of the upper CN and N3 ligands are red-shifted 20−30 cm-1 from the ground-state frequencies, consistent with a weakened Co−upper ligand bond. These results suggest that the transient intermediate state can be attributed to a corrin ring π to Co 3d z 2 ligand to metal charge transfer (LMCT) state. In this state bonds between the cobalt and the axial ligands are weakened and lengthened with respect to the corresponding ground states.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja054374+</identifier><identifier>PMID: 16417369</identifier><identifier>CODEN: JACSAT</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Biological and medical sciences ; Electronic structure ; Fundamental and applied biological sciences. Psychology ; Hydroxocobalamin - chemistry ; Molecular biophysics ; Solvents ; Spectrophotometry, Infrared ; Spectrophotometry, Ultraviolet ; Structure in molecular biology ; Vitamin B 12 - analogs & derivatives ; Vitamin B 12 - chemistry</subject><ispartof>Journal of the American Chemical Society, 2006-01, Vol.128 (3), p.801-808</ispartof><rights>Copyright © 2006 American Chemical Society</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17730930$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16417369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shiang, Joseph J</creatorcontrib><creatorcontrib>Cole, Allwyn G</creatorcontrib><creatorcontrib>Sension, Roseanne J</creatorcontrib><creatorcontrib>Hang, Kun</creatorcontrib><creatorcontrib>Weng, Yuxiang</creatorcontrib><creatorcontrib>Trommel, Jenna S</creatorcontrib><creatorcontrib>Marzilli, Luigi G</creatorcontrib><creatorcontrib>Lian, Tianquan</creatorcontrib><title>Ultrafast Excited-State Dynamics in Vitamin B12 and Related Cob(III)alamins</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>Femtosecond transient IR and visible absorption spectroscopies have been employed to investigate the excited-state photophysics of vitamin B12 (cyanocobalamin, CNCbl) and the related cob(III)alamins, azidocobalamin (N3Cbl), and aquocobalamin (H2OCbl). Excitation of CNCbl, H2OCbl, or N3Cbl results in rapid formation of a short-lived excited state followed by ground-state recovery on time scales ranging from a few picoseconds to a few tens of picoseconds. The lifetime of the intermediate state is influenced by the σ-donating ability of the axial ligand, decreasing in the order CNCbl > N3Cbl > H2OCbl, and by the polarity of the solvent, decreasing with increasing solvent polarity. The peak of the excited-state visible absorption spectrum is shifted to ca. 490 nm, and the shape of the spectrum is characteristic of weak axial ligands, similar to those observed for cob(II)alamin, base-off cobalamins, or cobinamides. Transient IR spectra of the upper CN and N3 ligands are red-shifted 20−30 cm-1 from the ground-state frequencies, consistent with a weakened Co−upper ligand bond. These results suggest that the transient intermediate state can be attributed to a corrin ring π to Co 3d z 2 ligand to metal charge transfer (LMCT) state. In this state bonds between the cobalt and the axial ligands are weakened and lengthened with respect to the corresponding ground states.</description><subject>Biological and medical sciences</subject><subject>Electronic structure</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hydroxocobalamin - chemistry</subject><subject>Molecular biophysics</subject><subject>Solvents</subject><subject>Spectrophotometry, Infrared</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Structure in molecular biology</subject><subject>Vitamin B 12 - analogs & derivatives</subject><subject>Vitamin B 12 - chemistry</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNpF0d1LAkEQAPAlijTroX8g7qGiiKv9uP3wscxMkgq_6G0Z9_bg7DztdgX971tR62lmmB8DM4PQOcH3BFPyMAXMEyaTuwNUJ5zimBMqDlEdY0xjqQSroRPnpqFMqCLHqEZEQiQTzTp6GxW-ggycj9ork3ubxgMP3kbP6xJmuXFRXkbj3Ie8jJ4IjaBMo74tAkmj1nxy0-12b6HYtN0pOsqgcPZsFxto9NIetl7j3ken23rsxUCV9DEICilPUsMFsITxpsx4WIBby5VQVBLOqOQAxlrFOE5UlihsDDcTSXlTEdZA19u5i2r-s7TO61nujC0KKO186bTEEmNJVIAXO7iczGyqF1U-g2qt9-sHcLUD4AwUWQWlyd2_k5LhJsPBxVuXO29Xf32ovrWQTHI9_BzoMe-M--JrrN-Dv9x6ME5P58uqDPfQBOvNu_T-XewXxhN_7g</recordid><startdate>20060125</startdate><enddate>20060125</enddate><creator>Shiang, Joseph J</creator><creator>Cole, Allwyn G</creator><creator>Sension, Roseanne J</creator><creator>Hang, Kun</creator><creator>Weng, Yuxiang</creator><creator>Trommel, Jenna S</creator><creator>Marzilli, Luigi G</creator><creator>Lian, Tianquan</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20060125</creationdate><title>Ultrafast Excited-State Dynamics in Vitamin B12 and Related Cob(III)alamins</title><author>Shiang, Joseph J ; Cole, Allwyn G ; Sension, Roseanne J ; Hang, Kun ; Weng, Yuxiang ; Trommel, Jenna S ; Marzilli, Luigi G ; Lian, Tianquan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a287t-a62ad54dc56a343597f5a055ee586827153275aacee835048f480cc5cb7259813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Biological and medical sciences</topic><topic>Electronic structure</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hydroxocobalamin - chemistry</topic><topic>Molecular biophysics</topic><topic>Solvents</topic><topic>Spectrophotometry, Infrared</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Structure in molecular biology</topic><topic>Vitamin B 12 - analogs & derivatives</topic><topic>Vitamin B 12 - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shiang, Joseph J</creatorcontrib><creatorcontrib>Cole, Allwyn G</creatorcontrib><creatorcontrib>Sension, Roseanne J</creatorcontrib><creatorcontrib>Hang, Kun</creatorcontrib><creatorcontrib>Weng, Yuxiang</creatorcontrib><creatorcontrib>Trommel, Jenna S</creatorcontrib><creatorcontrib>Marzilli, Luigi G</creatorcontrib><creatorcontrib>Lian, Tianquan</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shiang, Joseph J</au><au>Cole, Allwyn G</au><au>Sension, Roseanne J</au><au>Hang, Kun</au><au>Weng, Yuxiang</au><au>Trommel, Jenna S</au><au>Marzilli, Luigi G</au><au>Lian, Tianquan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrafast Excited-State Dynamics in Vitamin B12 and Related Cob(III)alamins</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2006-01-25</date><risdate>2006</risdate><volume>128</volume><issue>3</issue><spage>801</spage><epage>808</epage><pages>801-808</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><coden>JACSAT</coden><abstract>Femtosecond transient IR and visible absorption spectroscopies have been employed to investigate the excited-state photophysics of vitamin B12 (cyanocobalamin, CNCbl) and the related cob(III)alamins, azidocobalamin (N3Cbl), and aquocobalamin (H2OCbl). Excitation of CNCbl, H2OCbl, or N3Cbl results in rapid formation of a short-lived excited state followed by ground-state recovery on time scales ranging from a few picoseconds to a few tens of picoseconds. The lifetime of the intermediate state is influenced by the σ-donating ability of the axial ligand, decreasing in the order CNCbl > N3Cbl > H2OCbl, and by the polarity of the solvent, decreasing with increasing solvent polarity. The peak of the excited-state visible absorption spectrum is shifted to ca. 490 nm, and the shape of the spectrum is characteristic of weak axial ligands, similar to those observed for cob(II)alamin, base-off cobalamins, or cobinamides. Transient IR spectra of the upper CN and N3 ligands are red-shifted 20−30 cm-1 from the ground-state frequencies, consistent with a weakened Co−upper ligand bond. These results suggest that the transient intermediate state can be attributed to a corrin ring π to Co 3d z 2 ligand to metal charge transfer (LMCT) state. In this state bonds between the cobalt and the axial ligands are weakened and lengthened with respect to the corresponding ground states.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16417369</pmid><doi>10.1021/ja054374+</doi><tpages>8</tpages></addata></record> |
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subjects | Biological and medical sciences Electronic structure Fundamental and applied biological sciences. Psychology Hydroxocobalamin - chemistry Molecular biophysics Solvents Spectrophotometry, Infrared Spectrophotometry, Ultraviolet Structure in molecular biology Vitamin B 12 - analogs & derivatives Vitamin B 12 - chemistry |
title | Ultrafast Excited-State Dynamics in Vitamin B12 and Related Cob(III)alamins |
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