Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Agnese Amati"'
Photosystem II is a large protein complex embedded in a phospholipid membrane. Photocatalytic water oxidation in liposomes using amphiphilic ruthenium(II)-trisbipyridine photosensitizer (PS) and amphiphilic 6,6’-dicarboxylato-2,2’-bipyridine-ruth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::5e59ae35461807ecdcd1ebf4461bcb74
https://zenodo.org/record/8029257
https://zenodo.org/record/8029257
Autor:
Pawel Jewula, Mickaël Grandmougin, Mélanie Choppin, Anna Maria Chiara Tivelli, Agnese Amati, Yoann Rousselin, Lydia Karmazin, Jean‐Claude Chambron, Michel Meyer
Publikováno v:
European Journal of Inorganic Chemistry
European Journal of Inorganic Chemistry, 2023, 26 (13), pp.e202300038. ⟨10.1002/ejic.202300038⟩
European Journal of Inorganic Chemistry, 2023, 26 (13), pp.e202300038. ⟨10.1002/ejic.202300038⟩
International audience; Six- and seven-membered cyclic hydroxamic acids are found as terminal binding units in different families of siderophores, including exochelins and mycobactins. The simplest models of these preorganized chelating ligands were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0da49f5bd3e33d622bf80bf76233530
https://hal.science/hal-04024384/document
https://hal.science/hal-04024384/document
Publikováno v:
Journal of the American Chemical Society, 144(42), 19353-19364. AMER CHEMICAL SOC
Photosystem II, the natural water-oxidizing system, is a large protein complex embedded in a phospholipid membrane. A much simpler system for photocatalytic water oxidation consists of liposomes functionalized with amphiphilic ruthenium(II)-trisbipyr
Aromatic amino acids such as l-tyrosine and l-tryptophan are deployed in natural systems to mediate electron transfer (ET) reactions. While tyrosine oxidation is always coupled to deprotonation (proton-coupled electron-transfer, PCET), both ET-only a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2879772d46d20edaa351de828f56ee4
https://hdl.handle.net/11392/2458042
https://hdl.handle.net/11392/2458042
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Aromatic amino acids such as l‐tyrosine and l‐tryptophan are deployed in natural systems to mediate electron transfer (ET) reactions. While tyrosine oxidation is always coupled to deprotonation (proton‐coupled electron‐transfer, PCET), both E
Publikováno v:
Journal of physical chemistry. C 124 (2020): 8514–8525. doi:10.1021/acs.jpcc.0c00224
info:cnr-pdr/source/autori:Natali, Mirco; Amati, Agnese; Merchiori, Sebastiano; Ventura, Barbara; Iengo, Elisabetta/titolo:Photoinduced Proton-Coupled Electron Transfer in Supramolecular Sn-IV Di(L-tyrosinato) Porphyrin Conjugates/doi:10.1021%2Facs.jpcc.0c00224/rivista:Journal of physical chemistry. C/anno:2020/pagina_da:8514/pagina_a:8525/intervallo_pagine:8514–8525/volume:124
info:cnr-pdr/source/autori:Natali, Mirco; Amati, Agnese; Merchiori, Sebastiano; Ventura, Barbara; Iengo, Elisabetta/titolo:Photoinduced Proton-Coupled Electron Transfer in Supramolecular Sn-IV Di(L-tyrosinato) Porphyrin Conjugates/doi:10.1021%2Facs.jpcc.0c00224/rivista:Journal of physical chemistry. C/anno:2020/pagina_da:8514/pagina_a:8525/intervallo_pagine:8514–8525/volume:124
Proton-coupled electron transfer (PCET) plays a key role in many biological processes, and a thorough comprehension of its subtle mechanistic complexity requires the synthesis and characterization of suitable artificial systems capable of mimicking t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ba8e29467f73e983f057d4215227840
http://hdl.handle.net/11392/2419234
http://hdl.handle.net/11392/2419234
Publikováno v:
Chemphyschem : a European journal of chemical physics and physical chemistry. 20(17)
A side-to-face array DPy-gPBI[Ru(4-tBuTPP)(CO)]
Autor:
Maria Teresa Indelli, Mirco Natali, Paolo Cavigli, Elisabetta Iengo, Agnese Amati, Nicola Demitri
A series of four arrays made of a central Sn(IV) porphyrin as scaffold axially connected, via carboxylate functions, to two free-base porphyrins has been prepared and fully characterized. Three arrays in the series feature the same free-base unit and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9391b42bbc1c2eea92f2826cff01304f
https://hdl.handle.net/11368/2990201
https://hdl.handle.net/11368/2990201
Autor:
Gabriele Balducci, Nicola Demitri, Ennio Zangrando, Paolo Cavigli, Elisabetta Iengo, Maria Teresa Indelli, Agnese Amati
Publikováno v:
Inorganica Chimica Acta. 439:61-68
We report here the synthesis, solution and solid state (single crystal X-ray structure) of a novel robust conjugate, obtained via axial coordination of two Re(diimine) fragments to one tin(IV) porphyrin center. The photophysical behavior of the conju
The novel conjugate 1, featuring two l-tyrosinato residues axially coordinated to the tin centre of a Sn(iv)- tetraphenylporphyrin, is reported as the first example of a supramolecular dyad for photochemical PCET. It is noteworthy that the excitation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::313a2a3557d265fffcfab157a546c0b2
https://pubs.rsc.org/en/Content/ArticleLanding/2018/CC/C8CC03441A
https://pubs.rsc.org/en/Content/ArticleLanding/2018/CC/C8CC03441A