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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
Main Authors: Shiang, Joseph J, Cole, Allwyn G, Sension, Roseanne J, Hang, Kun, Weng, Yuxiang, Trommel, Jenna S, Marzilli, Luigi G, Lian, Tianquan
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container_issue 3
container_start_page 801
container_title Journal of the American Chemical Society
container_volume 128
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.
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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 &gt; N3Cbl &gt; 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. 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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 &gt; N3Cbl &gt; 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. 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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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