Cargando…

Recent Progress in Research on [2.2]Paracyclophane-Based Dyes

In recent years, the [2.2]paracyclophane (PCP) ring has attracted extensive attention due to its features of providing not only chirality and electron-donating ability but also steric hindrance, which reduces intermolecular π–π stacking interactions and thereby improves the fluorescence properties o...

Descripción completa

Detalles Bibliográficos
Autores principales:	Liu, Wenjing, Li, Huabin, Huo, Yanmin, Yao, Qingxia, Duan, Wenzeng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095835/ https://www.ncbi.nlm.nih.gov/pubmed/37049653 http://dx.doi.org/10.3390/molecules28072891

Ejemplares similares

4-Amino-12-methylsulfonyloxy-[2.2]paracyclophane
por: Meng, Xiangchao, et al.
Publicado: (2013)

5-Benzoyl-13-bromo-4-hydroxy[2.2]paracyclophane
por: Ma, Kelin, et al.
Publicado: (2012)

Regioselective Functionalization of [2.2]Paracyclophanes: Recent Synthetic Progress and Perspectives
por: Hassan, Zahid, et al.
Publicado: (2019)

4-Amino-13-(1-naphthyl)-[2,2]paracyclophane
por: Sun, Junshan, et al.
Publicado: (2008)

12,12′-[2,2′-Oxybis(ethane-2,1-diyl)bis(oxy)]bis[(R (p))-4-bromo[2.2]paracyclophane]
por: Hong, Bing, et al.
Publicado: (2011)

[2.2]Paracyclophane derivatives containing tetrathiafulvalene moieties
por: Sarbu, Laura G, et al.
Publicado: (2015)

An Approach to Paracyclophane-Based Tetrathiafulvalenes: Synthesis and Characterization of a Pseudo-Geminal [2.2]Paracyclophane 1,3-Dithia-2-Thione
por: Bahrin, Lucian G., et al.
Publicado: (2020)

Intraannular photoreactions in pseudo-geminally substituted [2.2]paracyclophanes
por: Hopf, Henning, et al.
Publicado: (2011)

Enantiospecific synthesis of [2.2]paracyclophane-4-thiol and derivatives
por: Rowlands, Gareth J, et al.
Publicado: (2009)

Building complex carbon skeletons with ethynyl[2.2]paracyclophanes
por: Dix, Ina, et al.
Publicado: (2014)

Selenium halide-induced bridge formation in [2.2]paracyclophanes
por: Sarbu, Laura G, et al.
Publicado: (2014)

[2.2]Paracyclophane Derivatives as Building Blocks for Coordination Polymers
por: Birsa, Mihail Lucian, et al.
Publicado: (2023)

4,12-Bis(2,2-dibromovinyl)[2.2]paracyclophane
por: Clément, Sébastien, et al.
Publicado: (2009)

Five-membered ring annelation in [2.2]paracyclophanes by aldol condensation
por: Hopf, Henning, et al.
Publicado: (2014)

Chiral isothiourea-catalyzed kinetic resolution of 4-hydroxy[2.2]paracyclophane
por: Weinzierl, David, et al.
Publicado: (2021)

Substitution Pattern Controlled Quantum Interference in [2.2]Paracyclophane-Based Single-Molecule Junctions
por: Reznikova, Ksenia, et al.
Publicado: (2021)

Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)
por: Dix, Ina, et al.
Publicado: (2010)

The preparation of new functionalized [2.2]paracyclophane derivatives with N-containing functional groups
por: Hopf, Henning, et al.
Publicado: (2015)

π-Stacked Polymer Consisting of a Pseudo–meta–[2.2]Paracyclophane Skeleton
por: Maeda, Hazuki, et al.
Publicado: (2018)

Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates with Pyridyl and Pyrimidyl Building Blocks
por: Knoll, Daniel M., et al.
Publicado: (2018)

A Luminescent 1D Silver Polymer Containing [2.2]Paracyclophane Ligands
por: Mackenzie, Campbell F. R., et al.
Publicado: (2021)

Breaking paracyclophane: the unexpected formation of non-symmetric disubstituted nitro[2.2]metaparacyclophanes
por: Patel, Suraj, et al.
Publicado: (2021)

Kinetic resolution of substituted amido[2.2]paracyclophanes via asymmetric electrophilic amination
por: Yu, Shaoze, et al.
Publicado: (2023)

Influencing the Self‐Sorting Behavior of [2.2]Paracyclophane‐Based Ligands by Introducing Isostructural Binding Motifs
por: Volbach, Lucia, et al.
Publicado: (2020)

[2,2] Paracyclophanes-based double helicates for constructing artificial light-harvesting systems and white LED device
por: Lian, Zhe, et al.
Publicado: (2023)

A new protocol for the synthesis of 4,7,12,15-tetrachloro[2.2]paracyclophane
por: Pan, Donghui, et al.
Publicado: (2016)

Circular Dichroisms of Mono- and Dibromo[2.2]paracyclophanes: A Combined Experimental and Theoretical Study
por: Toda, Mitsunobu, et al.
Publicado: (2018)

The concise synthesis and resolution of planar chiral [2.2]paracyclophane oxazolines by C–H activation
por: Tewari, Shashank, et al.
Publicado: (2022)

[2.2]Paracyclophane-Based Chiral Platforms for Circularly Polarized Luminescence Fluorophores and Their Chiroptical Properties: Past and Future
por: Sugiura, Ken-ichi
Publicado: (2020)

[2.2]Paracyclophane‐Based TCN‐201 Analogs as GluN2A‐Selective NMDA Receptor Antagonists
por: Rajan, Remya, et al.
Publicado: (2021)

Synthesis and characterization of rigid [2.2]paracyclophane–porphyrin conjugates as scaffolds for fixed-distance bimetallic complexes
por: Knoll, Daniel M., et al.
Publicado: (2019)

Planar Chiral [2.2]Paracyclophane-Based Bisoxazoline Ligands and Their Applications in Cu-Mediated N–H Insertion Reaction
por: Knoll, Daniel M., et al.
Publicado: (2019)

Synthesis of New Planar-Chiral Linked [2.2]Paracyclophanes-N-([2.2]-Paracyclophanylcarbamoyl)-4-([2.2]Paracyclophanylcarboxamide, [2.2]Paracyclophanyl-Substituted Triazolthiones and -Substituted Oxadiazoles
por: Aly, Ashraf A., et al.
Publicado: (2020)

Design and synthesis of chiral and regenerable [2.2]paracyclophane-based NAD(P)H models and application in biomimetic reduction of flavonoids
por: Zhu, Zhou-Hao, et al.
Publicado: (2020)

Controlling Regioselectivity in Palladium‐Catalyzed C−H Activation/Aryl–Aryl Coupling of 4‐Phenylamino[2.2]paracyclophane
por: Zippel, Christoph, et al.
Publicado: (2020)

Synthesis, aggregation induced emission and through space conjugation of triphenylvinylphenyl substituted [2.2]paracyclophane-1,9-diene
por: Yu, Chin-Yang, et al.
Publicado: (2018)

Efficient Synthesis of Various Substituted (Thio)Ureas, Semicarbazides, Thiosemicarbazides, Thiazolidones, and Oxadiazole Derived from [2.2]Paracyclophane
por: Alshammari, Mohammed B., et al.
Publicado: (2022)

Bright Luminescence by Combining Chiral [2.2]Paracyclophane with a Boron–Nitrogen‐Doped Polyaromatic Hydrocarbon Building Block
por: Rapp, Mario R., et al.
Publicado: (2022)

Lemniscular carbon nanohoops with contiguous conjugation from planar chiral [2.2]paracyclophane: influence of the regioselective synthesis on topological chirality
por: He, Jing, et al.
Publicado: (2023)

Synthesis of a Ni Complex Chelated by a [2.2]Paracyclophane-Functionalized Diimine Ligand and Its Catalytic Activity for Olefin Oligomerization
por: Takeuchi, Daisuke, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_jb530835681l40i6ehnnd9f6ve