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Photochemical Reactivity of Naphthol-Naphthalimide Conjugates and Their Biological Activity

Photochemical Reactivity of Naphthol-Naphthalimide Conjugates and Their Biological Activity

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_89fce37d67524be5bab8ddccb3c1447f

Photochemical Reactivity of Naphthol-Naphthalimide Conjugates and Their Biological Activity

About this item

Full title

Photochemical Reactivity of Naphthol-Naphthalimide Conjugates and Their Biological Activity

Publisher

Basel: MDPI AG

Journal title

Molecules (Basel, Switzerland), 2021-06, Vol.26 (11), p.3355

Language

English

Formats

Publication information

Publisher

Basel: MDPI AG

More information

Scope and Contents

Contents

Quinone methide precursors 1a–e, with different alkyl linkers between the naphthol and the naphthalimide chromophore, were synthesized. Their photophysical properties and photochemical reactivity were investigated and connected with biological activity. Upon excitation of the naphthol, Förster resonance energy transfer (FRET) to the naphthalimide t...

Alternative Titles

Full title

Photochemical Reactivity of Naphthol-Naphthalimide Conjugates and Their Biological Activity

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_89fce37d67524be5bab8ddccb3c1447f

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_89fce37d67524be5bab8ddccb3c1447f

Other Identifiers

ISSN

1420-3049

E-ISSN

1420-3049

DOI

10.3390/molecules26113355

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