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1.
Faraday Discuss ; 228(0): 312-328, 2021 05 27.
Artigo em Inglês | MEDLINE | ID: mdl-33565544

RESUMO

We discuss our recently reported femtosecond (fs) X-ray emission spectroscopy results on the ligand dissociation and recombination in nitrosylmyoglobin (MbNO) in the context of previous studies on ferrous haem proteins. We also present a preliminary account of femtosecond X-ray absorption studies on MbNO, pointing to the presence of more than one species formed upon photolysis.


Assuntos
Heme , Ligantes , Fotólise , Análise Espectral , Raios X
2.
J Phys Chem Lett ; 14(37): 8360-8366, 2023 Sep 21.
Artigo em Inglês | MEDLINE | ID: mdl-37703207

RESUMO

Two-dimensional (2D) halide perovskites exhibit unique structural and optical properties because large organic molecular cations distort the perovskite structure and the excitons confined in the 2D layers are stable. Here, we report the temperature dependences of the absorption spectra, second harmonic generation (SHG) intensity, and lattice constants of 2D perovskite (BA)2(EA)2Pb3I10 single crystals, where BA is n-butylammonium and EA is ethylammonium. We found that the Urbach tail of the absorption spectrum significantly changes at around 200 K and that the change is correlated with the SHG intensity and the in-plane lattice distortion. We concluded that a random distribution of spontaneous polarizations in the ferroelectric phase modifies the linewidth of the band-edge exciton transition and is the cause of the anomalous temperature dependence of the steepness parameter of the Urbach tail.

3.
Nat Commun ; 11(1): 4145, 2020 08 18.
Artigo em Inglês | MEDLINE | ID: mdl-32811825

RESUMO

In haemoglobin the change from the low-spin (LS) hexacoordinated haem to the high spin (HS, S = 2) pentacoordinated domed deoxy-myoglobin (deoxyMb) form upon ligand detachment from the haem and the reverse process upon ligand binding are what ultimately drives the respiratory function. Here we probe them in the case of Myoglobin-NO (MbNO) using element- and spin-sensitive femtosecond Fe Kα and Kß X-ray emission spectroscopy at an X-ray free-electron laser (FEL). We find that the change from the LS (S = 1/2) MbNO to the HS haem occurs in ~800 fs, and that it proceeds via an intermediate (S = 1) spin state. We also show that upon NO recombination, the return to the planar MbNO ground state is an electronic relaxation from HS to LS taking place in ~30 ps. Thus, the entire ligand dissociation-recombination cycle in MbNO is a spin cross-over followed by a reverse spin cross-over process.


Assuntos
Heme/química , Hemoglobinas/química , Mioglobina/química , Heme/metabolismo , Hemoglobinas/metabolismo , Cinética , Ligantes , Modelos Moleculares , Mioglobina/metabolismo , Espectrometria por Raios X
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