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Mohamed Bourass

Observed names: Bourass Mohamed, Bourass Mohammed, Bourass, M, Bourass, M., Bourass, Mohamed, M. Bourass, Mohammed Bourass
Observed institutions: Mohammed V University, Centre National de la Recherche Scientifique, Université de Bordeaux, Institut des Sciences Moléculaires, Département de Chimie Moléculaire, CY Cergy Paris Université, Université Moulay Ismail de Meknes, Institut Polytechnique de Bordeaux, Université de Cergy-Pontoise, Laboratoire de Physicochimie des Polymères et des Interfaces, Physico-Chimie des Matériaux et des Électrolytes pour l’Énergie, Sidi Mohamed Ben Abdellah University, Université Grenoble Alpes
ORCID: 0000-0001-6801-7851
Observed ORCID: 0000-0001-6801-7851
OpenAlex ID: A5062134751
DFT and TD-DFT calculation of new thienopyrazine-based small molecules for organic solar cells
2016 · Mohamed Bourass, Adil Touimi Benjelloun, et al. · Chemistry Central Journal · 156
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DFT/TD-DFT characterization of conjugational electronic structures and spectral properties of materials based on thieno[3,2-b][1]benzothiophene for organic photovoltaic and solar cell applications
2017 · Mohamed Bourass, Adil Touimi Benjelloun, et al. · Journal of Saudi Chemical Society · 71
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Synthesis, Characterization, DFT Mechanistic Study, Antimicrobial Activity, Molecular Modeling, and ADMET Properties of Novel Pyrazole-isoxazoline Hybrids
2022 · Mohammed Chalkha, Hassan Nour, et al. · ACS Omega · 68
DFT theoretical investigations of π-conjugated molecules based on thienopyrazine and different acceptor moieties for organic photovoltaic cells
2013 · Mohammed Bourass, Adil Touimi Benjelloun, et al. · Journal of Saudi Chemical Society · 52
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The optoelectronic properties of organic materials based on triphenylamine that are relevant to organic solar photovoltaic cells
2017 · Mohamed Bourass, Adil Touimi Benjelloun, et al. · New Journal of Chemistry · 50
Computational design of new organic (D–π–A) dyes based on benzothiadiazole for photovoltaic applications, especially dye-sensitized solar cells
2020 · Rachid Kacimi, Mohamed Bourass, et al. · Research on Chemical Intermediates · 48
Investigation of Antileishmanial Activities of Acridines Derivatives against Promastigotes and Amastigotes Form of Parasites Using Quantitative Structure Activity Relationship Analysis
2016 · Samir Chtita, Mounir Ghamali, et al. · Advances in Physical Chemistry · 38
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Theoretical investigation on π-spacer effect of the D–π–A organic dyes for dye-sensitized solar cell applications: a DFT and TD-BHandH study
2019 · Souad El Mzioui, Si Mohamed Bouzzine, et al. · Journal of Molecular Modeling · 36
New organic dyes based on phenylenevinylene for solar cells: DFT and TD-DFT investigation
2017 · Aziz El alamy, Mohamed Bourass, et al. · Karbala International Journal of Modern Science · 33
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New organic materials based on D–π–A structure for application in dye-sensitized solar cells
2018 · Hayat Sadki, Mohamed Bourass, et al. · Research on Chemical Intermediates · 30
The optoelectronic properties of new dyes based on thienopyrazine
2017 · Mohamed Bourass, Adil Touimi Benjelloun, et al. · Comptes Rendus Chimie · 29
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The photophysical properties and electronic structures of bis[1]benzothieno[6,7- d :6′,7′- d ′]benzo[1,2- b :4,5- b ′]dithiophene (BBTBDT) derivatives as hole-transporting materials for organic light-emitting diodes (OLEDs)
2019 · Mohamed Bourass, Najia Komiha, et al. · New Journal of Chemistry · 26
Design, synthesis and characterization of functionalized pyrazole derivatives bearing amide and sulfonamide moieties from aza-aurones
2020 · Mohammed Chalkha, Mohamed Bakhouch, et al. · Journal of Chemical Sciences · 25
Structural and photophysical studies of triphenylamine-based nonlinear optical dyes: effects of π-linker moieties on the D-π-A structure
2019 · Mohamed Bourass, Aziz El Alamy, et al. · Comptes Rendus Chimie · 24
Molecular design of D–A–D conjugated molecules based on fluorene for organic solar cells
2019 · Rachid Kacimi, Tayed Abram, et al. · Optical and Quantum Electronics · 23
Surface Functionalization of Sulflower with Superhalogens Doping to Achieve Robustly Large Nonlinear Optical Response: Interactive Design Computation of New NLO Materials for Modern Electro-Optic Applications
2023 · Abida Anwar, Riaz Hussain, et al. · Polycyclic aromatic compounds · 22
The computational study of the electronic and optoelectronics properties of new materials based on thienopyrazine for application in dye solar cells
2016 · Bourass, M., Touimi Benjelloun, A., et al. · HAL · 21
3D-QSAR models to predict anti-cancer activity on a series of protein P38 MAP kinase inhibitors
2016 · El Ghalia Hadaji, Mohamed Bourass, et al. · Journal of Taibah University for Science · 15
Doping superalkalis on chlorine substituted coronene: Interactive design computation of new NLO materials for optoelectronics
2023 · Fazilat Bano, Junaid Yaqoob, et al. · Journal of Photochemistry and Photobiology A Chemistry · 13
Theoretical Studies by Using the DFT and TD-DFT of the effect of the bridge formed of thienopyrazine in solar cells
2015 · Bourass, M, Touimi Benjelloun, A., et al. · HAL · 12
DFT and TDDFT investigations of new thienopyrazine-based dyes for solar cells: Effects of electron donor groups
2013 · Mohamed Bourass, Anisa '. Fitria, et al. · Der pharma chemica · 12
A theoretical investigation of the optoelectronic performance of some new carbazole dyes
2019 · Souad El Mzioui, Si Mohamed Bouzzine, et al. · Journal of Computational Electronics · 8
Photo-physical effects of the chemical insertion of the dimethyl-amine moiety on the newly synthesized oligophenylene (OMPA)
2021 · M. Chemek, S. Ben Amor, et al. · Journal of Molecular Structure · 6
Elaboration of low-band-gap π-conjugated systems based on thieno[3,4-b]pyrazines
2019 · Nathalie Cheminet, Sandra L. Nogueira, et al. · Pure and Applied Chemistry · 6
Electronic structures and photophysical properties of carbazole‐ and thiophene‐based organic compounds used as hole‐injecting layer for organic light‐emitting diodes ( OLEDs )
2022 · Mohamed Bourass, Yohann Nicolas, et al. · The Canadian Journal of Chemical Engineering · 5
Works count: 42
Citation count: 845
H-index: 17
I10-index: 21
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