Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines

Ruthenium polypyridine complexes have proved to be useful caging groups for visible-light photodelivery of biomolecules. In most photoreactions, one ligand is expelled upon irradiation, yielding ruthenium mono-aqua complexes and no other photoproduct. In this work we show that a long-lived transient...

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Autores principales: Carrone, G., Zayat, L., Slep, L.D., Etchenique, R.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_14639076_v19_n3_p2140_Carrone
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spelling todo:paper_14639076_v19_n3_p2140_Carrone2023-10-03T16:16:55Z Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines Carrone, G. Zayat, L. Slep, L.D. Etchenique, R. Ruthenium polypyridine complexes have proved to be useful caging groups for visible-light photodelivery of biomolecules. In most photoreactions, one ligand is expelled upon irradiation, yielding ruthenium mono-aqua complexes and no other photoproduct. In this work we show that a long-lived transient photoproduct is generated when the ruthenium complexes involve indolamines. The spatial conformation of this species is compatible with a cyclic structure that contains both the amine and the normally non-coordinating aromatic ring coordinated to the ruthenium center. © 2017 the Owner Societies. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_14639076_v19_n3_p2140_Carrone
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description Ruthenium polypyridine complexes have proved to be useful caging groups for visible-light photodelivery of biomolecules. In most photoreactions, one ligand is expelled upon irradiation, yielding ruthenium mono-aqua complexes and no other photoproduct. In this work we show that a long-lived transient photoproduct is generated when the ruthenium complexes involve indolamines. The spatial conformation of this species is compatible with a cyclic structure that contains both the amine and the normally non-coordinating aromatic ring coordinated to the ruthenium center. © 2017 the Owner Societies.
format JOUR
author Carrone, G.
Zayat, L.
Slep, L.D.
Etchenique, R.
spellingShingle Carrone, G.
Zayat, L.
Slep, L.D.
Etchenique, R.
Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines
author_facet Carrone, G.
Zayat, L.
Slep, L.D.
Etchenique, R.
author_sort Carrone, G.
title Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines
title_short Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines
title_full Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines
title_fullStr Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines
title_full_unstemmed Transient photocyclization in ruthenium(II) polypyridine complexes of indolamines
title_sort transient photocyclization in ruthenium(ii) polypyridine complexes of indolamines
url http://hdl.handle.net/20.500.12110/paper_14639076_v19_n3_p2140_Carrone
work_keys_str_mv AT carroneg transientphotocyclizationinrutheniumiipolypyridinecomplexesofindolamines
AT zayatl transientphotocyclizationinrutheniumiipolypyridinecomplexesofindolamines
AT slepld transientphotocyclizationinrutheniumiipolypyridinecomplexesofindolamines
AT etcheniquer transientphotocyclizationinrutheniumiipolypyridinecomplexesofindolamines
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