Evidence map›Paper›PMID 41492139›Full record

ArticlePhotochemistry and photobiology

Photophysics of hydroxy-nitrobenzoic acid UV-MALDI matrices investigated via spectroscopic, photoacoustic, and luminescence techniques.

Oscar E Silva Rodriguez, Gabriela Petroselli, Pedro M David Gara, Hernán B Rodríguez, Rosa Erra-Balsells

Abstract read
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Article in Photochemistry and photobiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Oscar E Silva RodriguezDepartamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón II, 3er P., Ciudad Universitaria, Buenos Aires, Argentina.
Gabriela PetroselliDepartamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón II, 3er P., Ciudad Universitaria, Buenos Aires, Argentina.
Pedro M David GaraCentro de Investigaciones Ópticas (CIOp; CONICET-CIC-UNLP), Buenos Aires, Argentina.
Hernán B RodríguezInstituto de Química, Física de los Materiales, Medio Ambiente y Energía (INQUIMAE, UBA-CONICET), CONICET - Universidad de Buenos Aires, Buenos Aires, Argentina.
Rosa Erra-BalsellsDepartamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón II, 3er P., Ciudad Universitaria, Buenos Aires, Argentina.ORCID https://orcid.org/0009-0006-4689-112X

Funding

Agencia Nacional de Promoción Científica y Tecnológica 2016-0130Consejo Nacional de Investigaciones Científicas y Técnicas 100072COConsejo Nacional de Investigaciones Científicas y Técnicas 100366COUniversity of Buenos Aires 100055BAUniversity of Buenos Aires 100110BA
6 · The paper itself

Abstract

The photophysical behavior of novel UV-MALDI matrices belonging to the family of hydroxy-nitrobenzoic acids (HNBAs) was investigated in both acetonitrile and methanol solutions, as well as in the solid state, using spectroscopic, luminescence, and photoacoustic techniques. The study focused on the following positional isomers: 2-hydroxy-3-nitrobenzoic acid, 2-hydroxy-4-nitrobenzoic acid, 2-hydroxy-5-nitrobenzoic acid, 3-hydroxy-2-nitrobenzoic acid, 3-hydroxy-4-nitrobenzoic acid, 3-hydroxy-5-nitrobenzoic acid, 4-hydroxy-3-nitrobenzoic acid, and 5-hydroxy-2-nitrobenzoic acid. Most isomers exhibited strong solid-state absorption at the excitation wavelengths commonly used in UV-MALDI technique (>90% at 337 and 355 nm), high photostability, no detectable luminescence, and highly efficient excitation energy dissipation as prompt heat, resembling the behavior of calorimetric references under both N

Indexed as

calorimetric referenceprompt heat emissionradiationless decaysinglet oxygensolid UV absorption

Identifiers

PMID41492139
PMCPMC13575722

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.