Results 161 to 170 of about 12,440 (225)

Rose Bengal-Incorporated Supramolecular Gels as a Topical Platform for Localized Antimicrobial Photodynamic Therapy. [PDF]

Int J Mol Sci
Anguluri K, Bagherpour S, Calpena AC, Halbaut L, Espargaró A, Sabate R, Pérez-García L.   +6 more
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Laser-Induced Graphene from Commercial Inks and Dyes. [PDF]

Adv Sci (Weinh)
Dallinger A, Camerini R, Parlanti P, Gemmi M, Sankaran ST, Galliani M, Kunert B, Giorgi R, Greco F.   +8 more
europepmc   +1 more source

Introducing Photochemical Action Plots as a Tool for Unlocking On-Off Switchable Behavior in a Polymeric Eosin Y Photocatalyst. [PDF]

Angew Chem Int Ed Engl
Gillhuber S, Finch AK, Holloway JO, Frisch H, Weigend F, Barner-Kowollik C, Roesky PW.   +6 more
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Biradical-mediated synergistic electrocatalysis using metal-free redox molecular catalysts. [PDF]

Nat Commun
Fu D, Zhu J, Wang L, Liu R, Jiao L, Li Z, Zhang X, Yang L, Ou P, Wu J.   +9 more
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Strategic Brazilian Minerals Applied in the Photocatalytic Ozonation of Rhodamine B Using a Green Lithium Niobate Nanocatalyst Supported on Silica: Kinetic, Thermodynamic, Mechanism, Machine Learning, and Ecotoxicity Study. [PDF]

ACS Omega
da Costa ML, Dos Santos C, MorenoRuiz YP, Pavoski G, Tenório JAS, Romano Espinosa DC, de Oliveira JS.   +6 more
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Structural basis for ring-opening fluorescence by the RhoBAST RNA aptamer. [PDF]

Nucleic Acids Res
Siwik SH, Wierzba AJ, Lennon SR, Olenginski LT, Palmer AE, Batey RT.   +5 more
europepmc   +1 more source

Leveraging Noncovalent Interactions for the Binding of CO by a Weakly Lewis Acidic Borane. [PDF]

Angew Chem Int Ed Engl
Crumpton AE, McManus C, Aldridge S.
europepmc   +1 more source

[a, j]xanthene derivatives].

Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 1998
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Deep Red to NIR Emitting Xanthene Hybrids: Xanthene‐Hemicyanine Hybrids and Xanthene‐Coumarin Hybrids

ChemistrySelect, 2023
Abstract Xanthene dyes exhibit remarkable photophysical properties and photostability. Their ability to switch fluorescence on/off depending on the external environment makes them a promising candidate for imaging/sensing/tracking/labeling probes. However, their emission ≤600 nm and Stokes shift ∼34 nm restrict their use in biological
Zeba Khan, Nagaiyan Sekar
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Xanthene-Bridged Cofacial Bisporphyrins

Inorganic Chemistry, 2000
The synthesis and characterization of cofacial bisporphyrins juxtaposed by xanthene-bridged pillars are presented. The one-pot preparation of the xanthene dialdehyde avoids the lengthy bridge synthesis accompanying other cofacial porphyrin systems, thus allowing for the facile preparation of homobimetallic zinc (10), copper (11), and nickel (12 ...
C J, Chang, Y, Deng, A F, Heyduk, C K, Chang, D G, Nocera   +4 more
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