Cargando…

D-π-A-Type Pyrazolo[1,5-a]pyrimidine-Based Hole-Transporting Materials for Perovskite Solar Cells: Effect of the Functionalization Position

Donor–acceptor (D–A) small molecules are regarded as promising hole-transporting materials for perovskite solar cells (PSCs) due to their tunable optoelectronic properties. This paper reports the design, synthesis and characterization of three novel isomeric D-π-A small molecules PY1, PY2 and PY3. T...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bouihi, Fatiha, Schmaltz, Bruno, Mathevet, Fabrice, Kreher, David, Faure-Vincent, Jérôme, Yildirim, Ceren, Elhakmaoui, Ahmed, Bouclé, Johann, Akssira, Mohamed, Tran-Van, François, Abarbri, Mohamed
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697137/ https://www.ncbi.nlm.nih.gov/pubmed/36431477 http://dx.doi.org/10.3390/ma15227992

Ejemplares similares

Efficient microwave-assisted Suzuki–Miyaura cross-coupling reaction of 3-bromo pyrazolo[1,5-a]pyrimidin-5(4H)-one: towards a new access to 3,5-diarylated 7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine derivatives
por: Jismy, Badr, et al.
Publicado: (2021)

Efficient Access to 3,5-Disubstituted 7-(Trifluoromethyl)pyrazolo[1,5-a]pyrimidines Involving S(N)Ar and Suzuki Cross-Coupling Reactions
por: Jismy, Badr, et al.
Publicado: (2020)

Unusual rearrangement of imidazo[1,5-a]imidazoles and imidazo[1,2-b]pyrazoles into imidazo[1,5-a]pyrimidines and pyrazolo[1,5-a]pyrimidines
por: Gambouz, Khadija, et al.
Publicado: (2019)

Electrical and Optical Properties of CaTi(1−y)Fe(y)O(3−δ) Perovskite Films as Interlayers for Optoelectronic Applications
por: Yildirim, Ceren, et al.
Publicado: (2022)

4-Benzylsulfanyl-1H-pyrazolo[3,4-d]pyrimidine
por: El Fal, Mohammed, et al.
Publicado: (2013)

Synthesis, characterization and in vitro antimicrobial activity of novel fused pyrazolo[3,4-c]pyridazine, pyrazolo[3,4-d]pyrimidine, thieno[3,2-c]pyrazole and pyrazolo[3′,4′:4,5]thieno[2,3-d]pyrimidine derivatives
por: Abdel Reheim, Mohamed A. M., et al.
Publicado: (2017)

Regioselective Synthesis of New 2,4-(Het)aryl-3H-pyrido[1′,2′:1,5]pyrazolo[4,3-d]pyrimidines Involving Palladium-Catalyzed Cross-Coupling Reactions
por: Ejjoummany, Abdelaziz, et al.
Publicado: (2018)

Correction to: Synthesis, characterization and in vitro antimicrobial activity of novel fused pyrazolo[3,4-c]pyridazine, pyrazolo[3,4-d]pyrimidine, thieno[3,2-c] pyrazole and pyrazolo[3′,4′:4,5]thieno[2,3-d]pyrimidine derivatives
por: Abdel Reheim, Mohamed A. M., et al.
Publicado: (2017)

Low-Temperature Hydrothermal Growth of ZnO Nanowires on AZO Substrates for FACsPb(IBr)(3) Perovskite Solar Cells
por: Sekar, Karthick, et al.
Publicado: (2022)

Design, Synthesis, and Antitumor Evaluation of Novel Pyrazolo[3,4-d]pyrimidine Derivatives
por: Kandeel, Manal M., et al.
Publicado: (2012)

Crystal structure of 4-allylsulfanyl-1H-pyrazolo[3,4-d]pyrimidine
por: El Fal, Mohammed, et al.
Publicado: (2014)

Discovery of pyrazolo[3,4-d]pyrimidine and pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine derivatives as novel CDK2 inhibitors: synthesis, biological and molecular modeling investigations
por: Nassar, Ibrahim F., et al.
Publicado: (2022)

2-Anilino-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-carbonitrile
por: Mohamed, Shaaban K., et al.
Publicado: (2012)

Cooperative effects between π-hole triel and π-hole chalcogen bonds
por: Zhang, Jingru, et al.
Publicado: (2018)

Novel star-shaped D–π–D–π–D and (D–π)(2)–D–(π–D)(2) anthracene-based hole transporting materials for perovskite solar cells
por: Harikrishnan, Muniyasamy, et al.
Publicado: (2020)

Efficient Synthesis of 1H-Benzo[4,5]imidazo[1,2-c][1,3]oxazin-1-one Derivatives Using Ag(2)CO(3)/TFA-Catalyzed 6-endo-dig Cyclization: Reaction Scope and Mechanistic Study
por: El Qami, Abdelkarim, et al.
Publicado: (2023)

4-Hydrazino-1-methylpyrazolo[3,4-d]pyrimidine
por: Dolzhenko, Anton V., et al.
Publicado: (2009)

Crystal structure of 1-ethylpyrazolo[3,4-d]pyrimidine-4(5H)-thione
por: El Fal, Mohammed, et al.
Publicado: (2014)

Synthesis, biological evaluation, and in silico studies of new CDK2 inhibitors based on pyrazolo[3,4-d]pyrimidine and pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine scaffold with apoptotic activity
por: Mandour, Asmaa A., et al.
Publicado: (2022)

Synthesis and Anticancer Activity of Some New Pyrazolo[3,4-d]pyrimidin-4-one Derivatives
por: Abdellatif, Khaled R. A., et al.
Publicado: (2014)

(Z)-6-Hydroxy-1a,5-dimethyl-8-[(morpholin-4-yl)methyl]-2,3,6,7,7a,8,10a,10b-octahydrooxireno[2′,3′:9,10]cyclodeca[1,2-b]furan-9(1aH)-one
por: Moumou, Mohamed, et al.
Publicado: (2011)

5,9-Dihydroxy-9-methyl-3,6-dimethylene-3a,4,5,6,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2(3H)-one
por: Moumou, Mohamed, et al.
Publicado: (2011)

5,8-Dimethyl-3-methylene-2-oxo-3,3a,4,5,5a,6,8a,8b-octahydro-2H-1-oxa-s-indacene-5-carbaldehyde
por: Moumou, Mohamed, et al.
Publicado: (2011)

Methyl 2-(3a,8a-dimethyl-4-oxodecahydroazulen-6-yl)acrylate
por: Tebbaa, Mohamed, et al.
Publicado: (2011)

(1S,2R,3R,8R,10S)-3-Chloro-2,8-dihydroxy-3,7-dimethyl-11-methylidene-13-oxabicyclo[8.3.0]tridec-6-en-12-one
por: Moumou, Mohamed, et al.
Publicado: (2011)

α-Costic anhydride
por: Tebbaa, Mohamed, et al.
Publicado: (2010)

2-Isopropyl-4-methoxy-5-methylphenyl benzoate
por: Moumou, Mohamed, et al.
Publicado: (2010)

1-(4a,8-Dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-2-yl)-3-phenylprop-2-en-1-one
por: Tebbaa, Mohamed, et al.
Publicado: (2011)

3-[4-(Dimethylamino)phenyl]-1-(4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-2-yl)prop-2-en-1-one
por: Tebbaa, Mohamed, et al.
Publicado: (2010)

1-[(2R,4aR,8R,8aR)-8-Hydroxy-4a,8-dimethylperhydronaphthalen-2-yl]ethan-1-one
por: Tebbaa, Mohamed, et al.
Publicado: (2011)

Crystal structure of 1-methyl-4-methylsulfanyl-1H-pyrazolo[3,4-d]pyrimidine
por: El Fal, Mohammed, et al.
Publicado: (2014)

Exploration of Pyrazolo[1,5‐a]pyrimidines as Membrane‐Bound Pyrophosphatase Inhibitors
por: Johansson, Niklas G., et al.
Publicado: (2021)

Three successive and regiocontroled palladium cross-coupling reactions to easily synthesize novel series of 2,4,6-tris(het)aryl pyrido[1′,2′:1,5]pyrazolo[3,4-d]pyrimidines
por: Belaroussi, R., et al.
Publicado: (2018)

Dopant-Free π-Conjugated Hole Transport Materials for Highly Stable and Efficient Perovskite Solar Cells
por: Deng, Zhifeng, et al.
Publicado: (2021)

Biological Evaluation and Molecular Docking with In Silico Physicochemical, Pharmacokinetic and Toxicity Prediction of Pyrazolo[1,5-a]pyrimidines
por: Naglah, Ahmed M., et al.
Publicado: (2020)

Simple and Expedient Access to Novel Fluorinated Thiazolo- and Oxazolo[3,2-a]pyrimidin-7-one Derivatives and Their Functionalization via Palladium-Catalyzed Reactions
por: Blancou, Wafa, et al.
Publicado: (2022)

Synthesis and Antimicrobial Activity of Some New Pyrazole, Fused Pyrazolo[3,4-d]-pyrimidine and Pyrazolo[4,3-e][1,2,4]-triazolo[1,5-c]pyrimidine Derivatives
por: Abunada, Nada M., et al.
Publicado: (2008)

Exploring the simultaneous σ-hole/π-hole bonding characteristics of a Br⋯π interaction in an ebselen derivative via experimental and theoretical electron-density analysis
por: Shukla, Rahul, et al.
Publicado: (2018)

Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: A complete structure–activity profile
por: Cacciari, Barbara, et al.
Publicado: (2006)

7-Chloro-5-methyl-2-phenylpyrazolo[1,5-a]pyrimidine
por: Bassoude, Ibtissam, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_71blfftdgfa73q7g0thcpnt1b3