3D Motions of Iron in Six-Coordinate {FeNO}7 Hemes by Nuclear Resonance Vibration Spectroscopy [3-D Motions of Iron in Six-coordinate {FeNO}7 Hemes by NRVS

Peng, Qian; Pavlik, Jeffrey W.; Silvernail, Nathan J.; Alp, E. Ercan; Hu, Michael Y.; Zhao, Jiyong; Sage, J. Timothy; Scheidt, W. Robert

doi:10.1002/chem.201505155

Title: 3D Motions of Iron in Six-Coordinate {FeNO}⁷ Hemes by Nuclear Resonance Vibration Spectroscopy [3-D Motions of Iron in Six-coordinate {FeNO}⁷ Hemes by NRVS

Journal Article · Mon Mar 21 00:00:00 EDT 2016 · Chemistry - A European Journal

DOI:https://doi.org/10.1002/chem.201505155· OSTI ID:1373306

Peng, Qian ^[1]; Pavlik, Jeffrey W. ^[1]; Silvernail, Nathan J. ^[1]; Alp, E. Ercan ^[2]; Hu, Michael Y. ^[2]; Zhao, Jiyong ^[2]; Sage, J. Timothy ^[3];

^[1]

Univ. of Notre Dame, Notre Dame, IN (United States)
Argonne National Lab. (ANL), Argonne, IL (United States)
Northeastern Univ., Boston, MA (United States)

Abstract The vibrational spectrum of a six‐coordinate nitrosyl iron porphyrinate, monoclinic [Fe(T p FPP)(1‐MeIm)(NO)] (T p FPP=tetra‐ para ‐fluorophenylporphyrin; 1‐MeIm=1‐methylimidazole), has been studied by oriented single‐crystal nuclear resonance vibrational spectroscopy (NRVS). The crystal was oriented to give spectra perpendicular to the porphyrin plane and two in‐plane spectra perpendicular or parallel to the projection of the FeNO plane. These enable assignment of the FeNO bending and stretching modes. The measurements reveal that the two in‐plane spectra have substantial differences that result from the strongly bonded axial NO ligand. The direction of the in‐plane iron motion is found to be largely parallel and perpendicular to the projection of the bent FeNO on the porphyrin plane. The out‐of‐plane Fe‐N‐O stretching and bending modes are strongly mixed with each other, as well as with porphyrin ligand modes. The stretch is mixed with v ₅₀ as was also observed for dioxygen complexes. The frequency of the assigned stretching mode of eight Fe‐X‐O (X=N, C, and O) complexes is correlated with the Fe−XO bond lengths. The nature of highest frequency band at ≈560 cm ⁻¹ has also been examined in two additional new derivatives. Previously assigned as the Fe−NO stretch (by resonance Raman), it is better described as the bend, as the motion of the central nitrogen atom of the FeNO group is very large. There is significant mixing of this mode. The results emphasize the importance of mode mixing; the extent of mixing must be related to the peripheral phenyl substituents.

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Research Organization:: Argonne National Laboratory (ANL), Argonne, IL (United States)

Sponsoring Organization:: National Institutes of Health (NIH); National Science Foundation (NSF); USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22), Scientific User Facilities Division; USDOE

Grant/Contract Number:: AC02-06CH11357

OSTI ID:: 1373306

Alternate ID(s):: OSTI ID: 1400744

Journal Information:: Chemistry - A European Journal, Vol. 22, Issue 18; ISSN 0947-6539

Publisher:: ChemPubSoc EuropeCopyright Statement

Country of Publication:: United States

Language:: English

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Cited by: 4 works

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Title: 3D Motions of Iron in Six-Coordinate {FeNO}⁷ Hemes by Nuclear Resonance Vibration Spectroscopy [3-D Motions of Iron in Six-coordinate {FeNO}⁷ Hemes by NRVS