Visible light-driven selective carbon–carbon bond formation for the production of vicinal diols

2020 ◽  
Vol 4 (11) ◽  
pp. 5488-5492
Author(s):  
Peng Bai ◽  
Xinli Tong ◽  
Yiqi Gao ◽  
Song Xue
Keyword(s):  
Visible Light ◽  
Visible Light Irradiation ◽  
Bond Formation ◽  
Light Irradiation ◽  
Carbon Bond ◽  
Benzylic Alcohols ◽  
Radical Coupling ◽  
Carbon Carbon Bond ◽  
Visible Light Driven ◽  
Vicinal Diols

A green and sustainable production of vicinal diols via the photocatalytic radical coupling of benzylic alcohols has been developed under visible light irradiation.

Visible light-driven novel g-C3N4/NiFe-LDH composite photocatalyst with enhanced photocatalytic activity towards water oxidation and reduction reaction

2015 ◽  
Vol 3 (36) ◽  
pp. 18622-18635 ◽  
Author(s):  
Susanginee Nayak ◽  
Lagnamayee Mohapatra ◽  
Kulamani Parida
Keyword(s):  
Photocatalytic Activity ◽  
Composite Materials ◽  
Visible Light ◽  
Water Splitting ◽  
Visible Light Irradiation ◽  
Water Oxidation ◽  
Reduction Reaction ◽  
Light Irradiation ◽  
Composite Photocatalyst ◽  
Visible Light Driven

Dispersion of exfoliated CN over the surface of exfoliated LDH composite materials, and its photocatalytic water splitting under visible-light irradiation.

Solvothermal synthesis and visible light-driven photocatalytic degradation for tetracycline of Fe-doped SrTiO3

RSC Advances ◽  
2014 ◽  
Vol 4 (88) ◽  
pp. 47615-47624 ◽  
Author(s):  
Ping Li ◽  
Chunbo Liu ◽  
Guoling Wu ◽  
Yang Heng ◽  
Shuang Lin ◽  
...  
Keyword(s):  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Solvothermal Synthesis ◽  
Solvothermal Method ◽  
Light Irradiation ◽  
Photocatalytic Activities ◽  
Visible Light Driven ◽  
Facile Solvothermal Method

In this paper, Fe-doped SrTiO3 (FSTO) photocatalysts were successfully prepared via a facile solvothermal method, and their photocatalytic activities for degrading tetracycline (TC) under visible light irradiation were examined.

Dehydrogenative 6π Heterocyclization under Visible Light Irradiation and Mechanistic Insights

2021 ◽  
Author(s):  
Zhao Zhang ◽  
Haohua Chen ◽  
Niklas Keller ◽  
Qin Xiong ◽  
Lei Liu ◽  
...  
Keyword(s):  
Transition Metals ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
Reaction Proceeds ◽  
Visible Light Driven

A visible-light-driven oxidative 6π heterocycilization for the synthesis of structurally diverse π-conjugated polycyclic 1-aminoisoquinolines has been developed. The reaction proceeds under visible-light or sunshine, obviates photocatalyst and transition-metals, and features...

scholarly journals Metal-free visible light photoredox enables generation of carbyne equivalents via phosphonium ylide C–H activation

2019 ◽  
Vol 10 (6) ◽  
pp. 1687-1691 ◽  
Author(s):  
Mrinmoy Das ◽  
Minh Duy Vu ◽  
Qi Zhang ◽  
Xue-Wei Liu
Keyword(s):  
Visible Light ◽  
Bond Formation ◽  
Formation Processes ◽  
New Approach ◽  
Carbon Bond ◽  
Metal Free ◽  
Carbon Carbon Bond ◽  
Carbon Carbon Bonds ◽  
Carbon Bonds ◽  
New Strategy

Phosphonium ylides have shown their synthetic usefulness in important carbon–carbon bond formation processes. Our new strategy employs phosphonium ylides as novel carbyne equivalents and features a new approach for constructing carbon–carbon bonds from alkenes.

Palladium chloride catalyzed photochemical Heck reaction

2013 ◽  
Vol 91 (5) ◽  
pp. 348-351 ◽  
Author(s):  
Suresh B. Waghmode ◽  
Sudhir S. Arbuj ◽  
Bina N. Wani ◽  
C.S. Gopinath
Keyword(s):  
Visible Light ◽  
Heck Reaction ◽  
Palladium Nanoparticles ◽  
Bond Formation ◽  
Aryl Halides ◽  
Palladium Chloride ◽  
Carbon Bond ◽  
Excellent Yield ◽  
Carbon Carbon Bond ◽  
Uv Visible

PdCl2 catalyzed carbon–carbon bond formation (Heck reaction) between substituted aryl halides and olefins was carried out without a ligand, under irradiation with UV–visible light. The results demonstrated that UV–visible light accelerated the rate of the reaction, leading to an excellent yield of corresponding products. The recovered palladium nanoparticles could be thermally recycled several times. PdCl2 gave excellent conversion up to the fifth addition of substrate.

Visible-light-driven photocatalysis of heterostructure Ag/Bi2WO6 nanocomposites and their photocatalytic degradation of dye under visible light irradiation

2015 ◽  
Vol 42 (3) ◽  
pp. 1651-1662 ◽  
Author(s):  
Phattranit Dumrongrojthanath ◽  
Anukorn Phuruangrat ◽  
Patcharanan Junploy ◽  
Somchai Thongtem ◽  
Titipun Thongtem
Keyword(s):  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
Visible Light Driven

Dechlorination of DDT catalyzed by visible-light-driven system composed of vitamin B12 derivative and Rhodamine B

2013 ◽  
Vol 17 (01n02) ◽  
pp. 135-141 ◽  
Author(s):  
Keishiro Tahara ◽  
Kumiko Mikuriya ◽  
Takahiro Masuko ◽  
Jun-ichi Kikuchi ◽  
Yoshio Hisaeda
Keyword(s):  
Visible Light ◽  
Visible Light Irradiation ◽  
Rhodamine B ◽  
Cobalt Complex ◽  
Light Irradiation ◽  
Vitamin B ◽  
Free Process ◽  
Driven System ◽  
Derivative System ◽  
Visible Light Driven

The visible-light-driven dechlorination of 1,1-bis(4-chlorophenyl)-2,2,2-trichloroethane (DDT) was carried out in the presence of a hydrophobic vitamin B12 , heptamethyl cobyrinate perchlorate and Rhodamine B . DDT was successfully dechlorinated to form 1,1-bis(4-chlorophenyl)-2,2-dichloroethane (DDD) as the mono-dechlorinated product upon visible light irradiation with a tungsten lamp (λ > 440 nm). Upon prolonged visible light irradiation to DDT, DDMU (1-chloro-2,2-bis(4-chlorophenyl)ethylene), DDMS (1-chloro-2,2-bis(4-chlorophenyl)ethane) and DCS (trans-4,4′-dichlorostilbene) were obtained as the di- and tri-dechlorinated products. The use of the photostable organic sensitizer enabled prolonged photocatalysis via a noble-metal-free process. The vitamin B12 derivative was replaced by an imine/oxime-type cobalt complex although the cobalt complex system showed a lower catalytic activity than the B12 derivative system. The dechlorination mechanism in the B12 -Rhodamin B system was investigated by various methods such as UV-vis absorption and fluorescence quenching.

The effect of molecular structure and fluorination on the properties of pyrene-benzothiadiazole-based conjugated polymers for visible-light-driven hydrogen evolution

2018 ◽  
Vol 9 (35) ◽  
pp. 4468-4475 ◽  
Author(s):  
Chang Cheng ◽  
Xunchang Wang ◽  
Yaoyao Lin ◽  
Luying He ◽  
Jia-Xing Jiang ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Visible Light ◽  
Conjugated Polymers ◽  
Hydrogen Evolution ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
Evolution Rate ◽  
Fluorinated Polymer ◽  
Hydrogen Evolution Rate ◽  
Visible Light Driven

The linear non-fluorinated polymer L-PyBT exhibited an impressive hydrogen evolution rate up to 83.7 μmol h−1 under visible light irradiation.

N-Loaded TiO2 for Photocatalytic Degradation of Methyl Orange under Visible Light Irradiation

2012 ◽  
Vol 622-623 ◽  
pp. 883-888
Author(s):  
Natkritta Boonprakob ◽  
Natda Wetchakun ◽  
Sukon Phanichphant ◽  
Jun Chen ◽  
Burapat Inceesungvorn
Keyword(s):  
Methyl Orange ◽  
Visible Light ◽  
Band Gap ◽  
Visible Light Irradiation ◽  
Sol Gel ◽  
Band Gap Energy ◽  
Light Irradiation ◽  
Gap Energy ◽  
Visible Light Driven ◽  
Degradation Of Methyl Orange

Nitrogen-loaded TiO2(N-loaded TiO2), a visible-light driven catalyst, was successfully synthesized by the modified sol-gel method. Physical characterizations of the as-prepared catalysts have been performed by using X-ray diffraction (XRD), Diffuse reflectance UVvisspectroscopy(DRUVvis), Raman spectroscopyand BETspecific surface areain order to obtain structure-activity relationship. Results from Raman spectroscopy clearly suggested that N atoms were incorporated into the TiO2crystal lattice as evidenced by the vibrational peak of TiN in TiO2-xNx.DR UVvis results also suggested that the nitrogen dopant might be responsible for narrowing the TiO2band gap energy, thus resulting in a shift towards the visiblelight region. Photocatalytic activity of N-loaded TiO2evaluated through the degradation of methyl orange (MO)under visible light irradiation (l> 400 nm) indicated that all N-loaded photocatalysts exhibited significantly higher activities than the unloaded TiO2and Degussa P25 TiO2. According to the results from DR UV-vis, XRD and BET studies, the enhanced photoactivity observed from N-loaded samples might be due to a decrease in TiO2band gap energy and/or changes in chemical and physical properties of the materials upon loading with nitrogen.

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