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פותח על ידי קלירמאש פתרונות בע"מ -
Evidence for a terminal Pt(iv)-oxo complex exhibiting diverse reactivity
Year:
2008
Source of publication :
Nature
Authors :
פוברנוב, ילנה
;
.
Volume :
455
Co-Authors:
Poverenov, E., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Efremenko, I., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Frenkel, A.I., Department of Physics, Yeshiva University, New York, NY 10016, United States
Ben-David, Y., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Shimon, L.J.W., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot 76100, Israel
Leitus, G., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot 76100, Israel
Konstantinovski, L., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot 76100, Israel
Martin, J.M.L., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Milstein, D., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Facilitators :
From page:
1093
To page:
1096
(
Total pages:
4
)
Abstract:
Terminal oxo complexes of transition metals have critical roles in various biological and chemical processes. For example, the catalytic oxidation of organic molecules, some oxidative enzymatic transformations, and the activation of dioxygen on metal surfaces are all thought to involve oxo complexes. Moreover, they are believed to be key intermediates in the photocatalytic oxidation of water to give molecular oxygen, a topic of intensive global research aimed at artificial photosynthesis and water splitting. The terminal oxo ligand is a strong π-electron donor, so it readily forms stable complexes with high-valent early transition metals. As the d orbitals are filled up with valence electrons, the terminal oxo ligand becomes destabilized. Here we present evidence for a dn (n > 5) terminal oxo complex that is not stabilized by an electron withdrawing ligand framework. This d6 Pt(iv) complex exhibits reactivity as an inter- and intramolecular oxygen donor and as an electrophile. In addition, it undergoes a water activation process leading to a terminal dihydroxo complex, which may be relevant to the mechanism of catalytic reactions such as water oxidation. ©2008 Macmillan Publishers Limited. All rights reserved.
Note:
Related Files :
article
catalysis
electron
enzyme activity
ligand
molecular interaction
oxidation
photosynthesis
platinum derivative
עוד תגיות
תוכן קשור
More details
DOI :
10.1038/nature07356
Article number:
Affiliations:
Database:
סקופוס
Publication Type:
מאמר
;
.
Language:
אנגלית
Editors' remarks:
ID:
18920
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:25
You may also be interested in
Scientific Publication
Evidence for a terminal Pt(iv)-oxo complex exhibiting diverse reactivity
455
Poverenov, E., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Efremenko, I., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Frenkel, A.I., Department of Physics, Yeshiva University, New York, NY 10016, United States
Ben-David, Y., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Shimon, L.J.W., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot 76100, Israel
Leitus, G., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot 76100, Israel
Konstantinovski, L., Unit of Chemical Research Support, Weizmann Institute of Science, Rehovot 76100, Israel
Martin, J.M.L., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Milstein, D., Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel
Evidence for a terminal Pt(iv)-oxo complex exhibiting diverse reactivity
Terminal oxo complexes of transition metals have critical roles in various biological and chemical processes. For example, the catalytic oxidation of organic molecules, some oxidative enzymatic transformations, and the activation of dioxygen on metal surfaces are all thought to involve oxo complexes. Moreover, they are believed to be key intermediates in the photocatalytic oxidation of water to give molecular oxygen, a topic of intensive global research aimed at artificial photosynthesis and water splitting. The terminal oxo ligand is a strong π-electron donor, so it readily forms stable complexes with high-valent early transition metals. As the d orbitals are filled up with valence electrons, the terminal oxo ligand becomes destabilized. Here we present evidence for a dn (n > 5) terminal oxo complex that is not stabilized by an electron withdrawing ligand framework. This d6 Pt(iv) complex exhibits reactivity as an inter- and intramolecular oxygen donor and as an electrophile. In addition, it undergoes a water activation process leading to a terminal dihydroxo complex, which may be relevant to the mechanism of catalytic reactions such as water oxidation. ©2008 Macmillan Publishers Limited. All rights reserved.
Scientific Publication
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