Two rhodamine 6G derivative compounds: A structural and fluorescence single-crystal study

The synthesis, characterization, structural analysis and fluorescence properties of two rhodamine 6G derivatives are described, namely a propargylamine derivative, 3′,6′-bis(ethylamino)-2′,7′-dimethyl-2-(methylcyanide)spiro[isoindole-1,9′-xanthen]-3(2H)-one (I), and a γ-aminobutyric acid (GABA) deri...

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Autores principales: Di Paolo, M., Bossi, M.L., Baggio, R., Suarez, S.A.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_20525192_v72_n_p684_DiPaolo
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spelling todo:paper_20525192_v72_n_p684_DiPaolo2023-10-03T16:38:56Z Two rhodamine 6G derivative compounds: A structural and fluorescence single-crystal study Di Paolo, M. Bossi, M.L. Baggio, R. Suarez, S.A. atoms in molecules theory fluorescence photocrystallography rhodamine 6G derivatives weak interactions Amino acids Fluorescence Molecules Single crystals Structural analysis Atoms in molecules theory Cambridge structural database Fluorescence properties Gamma-aminobutyric acids Photocrystallography Rhodamine 6G Single-crystal study Weak interactions Crystal atomic structure fluorescent dye rhodamine rhodamine 6G chemical structure chemistry fluorescence molecular model synthesis X ray crystallography Chemistry Techniques, Synthetic Crystallography, X-Ray Fluorescence Fluorescent Dyes Models, Molecular Molecular Structure Rhodamines The synthesis, characterization, structural analysis and fluorescence properties of two rhodamine 6G derivatives are described, namely a propargylamine derivative, 3′,6′-bis(ethylamino)-2′,7′-dimethyl-2-(methylcyanide)spiro[isoindole-1,9′-xanthen]-3(2H)-one (I), and a γ-aminobutyric acid (GABA) derivative, 3′,6′-bis(ethylamino)-2′,7′-dimethyl-3-oxospiro[isoindole-1,9′-xanthen]-2(3H)-yl)butyricacid (II). Both structures are compared with four similar ones from the Cambridge Structural Database (CSD), and the interactions involved in the stabilization are analyzed using the atoms in molecules (AIM) theory. Finally, a single-crystal in-situ reaction study is presented, carried out by fluorescence methods, which enabled the 'opening' of the spirolactam ring in the solid phase. © 2016 International Union of Crystallography. Fil:Di Paolo, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bossi, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Suarez, S.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_20525192_v72_n_p684_DiPaolo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic atoms in molecules theory
fluorescence
photocrystallography
rhodamine 6G derivatives
weak interactions
Amino acids
Fluorescence
Molecules
Single crystals
Structural analysis
Atoms in molecules theory
Cambridge structural database
Fluorescence properties
Gamma-aminobutyric acids
Photocrystallography
Rhodamine 6G
Single-crystal study
Weak interactions
Crystal atomic structure
fluorescent dye
rhodamine
rhodamine 6G
chemical structure
chemistry
fluorescence
molecular model
synthesis
X ray crystallography
Chemistry Techniques, Synthetic
Crystallography, X-Ray
Fluorescence
Fluorescent Dyes
Models, Molecular
Molecular Structure
Rhodamines
spellingShingle atoms in molecules theory
fluorescence
photocrystallography
rhodamine 6G derivatives
weak interactions
Amino acids
Fluorescence
Molecules
Single crystals
Structural analysis
Atoms in molecules theory
Cambridge structural database
Fluorescence properties
Gamma-aminobutyric acids
Photocrystallography
Rhodamine 6G
Single-crystal study
Weak interactions
Crystal atomic structure
fluorescent dye
rhodamine
rhodamine 6G
chemical structure
chemistry
fluorescence
molecular model
synthesis
X ray crystallography
Chemistry Techniques, Synthetic
Crystallography, X-Ray
Fluorescence
Fluorescent Dyes
Models, Molecular
Molecular Structure
Rhodamines
Di Paolo, M.
Bossi, M.L.
Baggio, R.
Suarez, S.A.
Two rhodamine 6G derivative compounds: A structural and fluorescence single-crystal study
topic_facet atoms in molecules theory
fluorescence
photocrystallography
rhodamine 6G derivatives
weak interactions
Amino acids
Fluorescence
Molecules
Single crystals
Structural analysis
Atoms in molecules theory
Cambridge structural database
Fluorescence properties
Gamma-aminobutyric acids
Photocrystallography
Rhodamine 6G
Single-crystal study
Weak interactions
Crystal atomic structure
fluorescent dye
rhodamine
rhodamine 6G
chemical structure
chemistry
fluorescence
molecular model
synthesis
X ray crystallography
Chemistry Techniques, Synthetic
Crystallography, X-Ray
Fluorescence
Fluorescent Dyes
Models, Molecular
Molecular Structure
Rhodamines
description The synthesis, characterization, structural analysis and fluorescence properties of two rhodamine 6G derivatives are described, namely a propargylamine derivative, 3′,6′-bis(ethylamino)-2′,7′-dimethyl-2-(methylcyanide)spiro[isoindole-1,9′-xanthen]-3(2H)-one (I), and a γ-aminobutyric acid (GABA) derivative, 3′,6′-bis(ethylamino)-2′,7′-dimethyl-3-oxospiro[isoindole-1,9′-xanthen]-2(3H)-yl)butyricacid (II). Both structures are compared with four similar ones from the Cambridge Structural Database (CSD), and the interactions involved in the stabilization are analyzed using the atoms in molecules (AIM) theory. Finally, a single-crystal in-situ reaction study is presented, carried out by fluorescence methods, which enabled the 'opening' of the spirolactam ring in the solid phase. © 2016 International Union of Crystallography.
format JOUR
author Di Paolo, M.
Bossi, M.L.
Baggio, R.
Suarez, S.A.
author_facet Di Paolo, M.
Bossi, M.L.
Baggio, R.
Suarez, S.A.
author_sort Di Paolo, M.
title Two rhodamine 6G derivative compounds: A structural and fluorescence single-crystal study
title_short Two rhodamine 6G derivative compounds: A structural and fluorescence single-crystal study
title_full Two rhodamine 6G derivative compounds: A structural and fluorescence single-crystal study
title_fullStr Two rhodamine 6G derivative compounds: A structural and fluorescence single-crystal study
title_full_unstemmed Two rhodamine 6G derivative compounds: A structural and fluorescence single-crystal study
title_sort two rhodamine 6g derivative compounds: a structural and fluorescence single-crystal study
url http://hdl.handle.net/20.500.12110/paper_20525192_v72_n_p684_DiPaolo
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AT bossiml tworhodamine6gderivativecompoundsastructuralandfluorescencesinglecrystalstudy
AT baggior tworhodamine6gderivativecompoundsastructuralandfluorescencesinglecrystalstudy
AT suarezsa tworhodamine6gderivativecompoundsastructuralandfluorescencesinglecrystalstudy
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