Cargando…

Photophysical Properties of Donor-Acceptor Stenhouse Adducts and Their Inclusion Complexes with Cyclodextrins and Cucurbit[7]uril

Donor-acceptor Stenhouse adducts (DASAs) are a novel class of solvatochromic photoswitches with increasing importance in photochemistry. Known for their reversibility between open triene and closed cyclized states, these push-pull molecules are applicable in a suite of light-controlled applications....

Descripción completa

Detalles Bibliográficos
Autores principales:	Payne, Liam, Josephson, Jason D., Murphy, R. Scott, Wagner, Brian D.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662831/ https://www.ncbi.nlm.nih.gov/pubmed/33114461 http://dx.doi.org/10.3390/molecules25214928

Ejemplares similares

Donor–acceptor Stenhouse adduct functionalised polymer microspheres
por: Wesseler, Justus P., et al.
Publicado: (2023)

Shedding Light on the Photoisomerization Pathway of Donor–Acceptor Stenhouse Adducts
por: Di Donato, Mariangela, et al.
Publicado: (2017)

Structure–function relationships of donor–acceptor Stenhouse adduct photochromic switches
por: Mallo, Neil, et al.
Publicado: (2018)

Construction and Properties of Donor–Acceptor Stenhouse Adducts on Gold Surfaces
por: Nánási, Dalma Edit, et al.
Publicado: (2021)

Two-photon isomerization properties of donor–acceptor Stenhouse adducts
por: Reza-González, Francisco A., et al.
Publicado: (2023)

Solvent Effects on the Actinic Step of Donor–Acceptor Stenhouse Adduct Photoswitching
por: Lerch, Michael M., et al.
Publicado: (2018)

New Donor-Acceptor Stenhouse Adducts as Visible and Near Infrared Light Polymerization Photoinitiators
por: Noirbent, Guillaume, et al.
Publicado: (2020)

Donor–acceptor Stenhouse adduct-grafted polycarbonate surfaces: selectivity of the reaction for secondary amine on surface
por: Singh, Sukhdeep, et al.
Publicado: (2018)

Taming the Complexity of Donor–Acceptor Stenhouse Adducts: Infrared Motion Pictures of the Complete Switching Pathway
por: Zulfikri, Habiburrahman, et al.
Publicado: (2019)

Promoting the Furan Ring‐Opening Reaction to Access New Donor–Acceptor Stenhouse Adducts with Hexafluoroisopropanol
por: Clerc, Michèle, et al.
Publicado: (2021)

Redesigning donor–acceptor Stenhouse adduct photoswitches through a joint experimental and computational study
por: Berraud-Pache, Romain, et al.
Publicado: (2021)

Mechanism of the Aza-Piancatelli Reaction: Scope and Limitations of Furan Substitution in Donor–Acceptor Stenhouse Adduct Synthesis
por: Peñín, Beatriz, et al.
Publicado: (2022)

Visible light-responsive materials: the (photo)chemistry and applications of donor–acceptor Stenhouse adducts in polymer science
por: Clerc, Michèle, et al.
Publicado: (2023)

Controlling the structure and photophysics of fluorophore dimers using multiple cucurbit[8]uril clampings
por: Wu, Guanglu, et al.
Publicado: (2019)

Cucurbit[6]uril p-xylylenediammonium diiodide decahydrate inclusion complex
por: Huang, Wei-Hao, et al.
Publicado: (2008)

Co-grinding Effect on Crystalline Zaltoprofen with β-cyclodextrin/Cucurbit[7]uril in Tablet Formulation
por: Li, Shanshan, et al.
Publicado: (2017)

Preparation, characterization, and biological activity study of thymoquinone-cucurbit[7]uril inclusion complex
por: Alrawashdeh, Lubna, et al.
Publicado: (2022)

Host-guest complexes of imazalil with cucurbit[8]uril and β-cyclodextrin and their effect on plant pathogenic fungi
por: Al-Dubaili, Naji, et al.
Publicado: (2018)

4-Sulfocalix[4]arene/Cucurbit[7]uril-Based Supramolecular Assemblies through the Outer Surface Interactions of Cucurbit[n]uril
por: Tian, Xiao, et al.
Publicado: (2018)

A LSER-based model to predict the solubilizing effect of drugs by inclusion with cucurbit[7]uril
por: Cheng, Enping, et al.
Publicado: (2020)

Encapsulation of Trimethine Cyanine in Cucurbit[8]uril: Solution versus Solid‐State Inclusion Behavior
por: Soavi, Giuseppe, et al.
Publicado: (2022)

Cucurbit[7]uril-based high-performance catalytic microreactors
por: Ren, Xiaohe, et al.
Publicado: (2018)

A systematic evaluation of the biocompatibility of cucurbit[7]uril in mice
por: Zhang, Xiangjun, et al.
Publicado: (2018)

Investigation on the hydrolytic mechanism of cucurbit[6]uril in alkaline solution
por: Zhu, Chao, et al.
Publicado: (2018)

A Method for Synthesizing Partially Substituted Cucurbit[n]uril
por: Day, Anthony I., et al.
Publicado: (2003)

Host-guest complexation of cucurbit[8]uril with two enantiomers
por: Gao, Zhong-Zheng, et al.
Publicado: (2017)

Assessment of Cooperativity in Ternary Peptide‐Cucurbit[8]uril Complexes
por: Cavatorta, Emanuela, et al.
Publicado: (2017)

Supramolecular Encapsulation of a Neurotransmitter Serotonin by Cucurbit[7]uril
por: Chandra, Falguni, et al.
Publicado: (2020)

Encapsulation of Cinnamic Acid by Cucurbit[7]uril for Enhancing Photoisomerization
por: Saleh, Na’il, et al.
Publicado: (2020)

Host–guest interaction and properties of cucurbit[8]uril with chloramphenicol
por: Zhang, Lin, et al.
Publicado: (2021)

Broad-Spectrum Extracellular Antiviral Properties of Cucurbit[n]urils
por: Jones, Luke M., et al.
Publicado: (2022)

Metal-Assisted Complexation of Fluorogenic Dyes by Cucurbit[7]uril and Cucurbit[8]uril: A DFT Evaluation of the Key Factors Governing the Host–Guest Recognition
por: Kircheva, Nikoleta, et al.
Publicado: (2023)

DFT-D4 Insight into the Inclusion of Amphetamine and Methamphetamine in Cucurbit[7]uril: Energetic, Structural and Biosensing Properties
por: Litim, Abdelkarim, et al.
Publicado: (2021)

The effect of permodified cyclodextrins encapsulation on the photophysical properties of a polyfluorene with randomly distributed electron-donor and rotaxane electron-acceptor units
por: Farcas, Aurica, et al.
Publicado: (2014)

Cucurbit[7]uril Complexation of Near-Infrared Fluorescent Azobenzene-Cyanine Conjugates
por: Kommidi, Sai Shradha Reddy, et al.
Publicado: (2022)

Toxicology and Drug Delivery by Cucurbit[n]uril Type Molecular Containers
por: Hettiarachchi, Gaya, et al.
Publicado: (2010)

Turning Cucurbit[8]uril into a Supramolecular Nanoreactor for Asymmetric Catalysis
por: Zheng, Lifei, et al.
Publicado: (2015)

Turning Cucurbit[8]uril into a Supramolecular Nanoreactor for Asymmetric Catalysis
por: Zheng, Lifei, et al.
Publicado: (2015)

Solubilization of Pyridone-Based Fluorescent Tag by Complexation in Cucurbit[7]uril
por: Alzard, Reem H., et al.
Publicado: (2019)

pH-Mediated Single Molecule Conductance of Cucurbit[7]uril
por: Ai, Qiushuang, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_a0lufl3ghio1iore33qpothlqn