scholarly journals Light-Induced Charge Transfer from Transition-Metal-Doped Aluminum Clusters to Carbon Dioxide

Author(s):  
Alexandra Göbel ◽  
Angel Rubio ◽  
Johannes Lischner
2021 ◽  
Vol 154 (5) ◽  
pp. 054312
Author(s):  
Jan Vanbuel ◽  
Piero Ferrari ◽  
Meiye Jia ◽  
André Fielicke ◽  
Ewald Janssens

2019 ◽  
Vol 25 (12) ◽  
Author(s):  
Kleuton Antunes Lopes Lima ◽  
Wiliam Ferreira da Cunha ◽  
Fábio Ferreira Monteiro ◽  
Bernhard Georg Enders ◽  
Marcelo Lopes Pereira Jr ◽  
...  

2015 ◽  
Vol 21 (21) ◽  
pp. 7780-7789 ◽  
Author(s):  
Jilai Li ◽  
Patricio González-Navarrete ◽  
Maria Schlangen ◽  
Helmut Schwarz

2021 ◽  
Vol 542 ◽  
pp. 148568
Author(s):  
Yanan Meng ◽  
Yan Gao ◽  
Kai Li ◽  
Hao Tang ◽  
Ying Wang ◽  
...  

1993 ◽  
Vol 143-147 ◽  
pp. 317-322 ◽  
Author(s):  
T. Wolf ◽  
W. Ulrici ◽  
D. Côte ◽  
B. Clerjaud ◽  
D. Bimberg

2016 ◽  
Vol 120 (18) ◽  
pp. 10027-10040 ◽  
Author(s):  
Turbasu Sengupta ◽  
Susanta Das ◽  
Sourav Pal

2015 ◽  
Vol 764-765 ◽  
pp. 47-50
Author(s):  
Amir Abidov ◽  
Bunyod Allabergenov ◽  
Fei Yi Xiao ◽  
Xing Jin ◽  
Soon Wook Jeong ◽  
...  

Capture and reforming fume gases from atmosphere became an ultimate task recently. Photocatalytic reduction to useful compounds is a key to the future. Photoinduced reduction of carbon dioxide and ammonia aqueous solution into amine compounds at room temperature and atmospheric pressure using transition metal doped titanium dioxide is reported in this paper. UV-visible spectra showed a high absorbance at 200 nm wavelength which is a characteristic of urea. High Performance Liquid Chromatography revealed presence of amine compounds and urea was found a main product of photocatalytic reaction.


2018 ◽  
Author(s):  
Mohit Kapoor ◽  
Pratibha Chand-Thakuri ◽  
Michael Young

Carbon-carbon bond formation by transition metal-catalyzed C–H activation has become an important strategy to fabricate new bonds in a rapid fashion. Despite the pharmacological importance of <i>ortho</i>-arylbenzylamines, however, effective <i>ortho</i>-C–C bond formation from C–H bond activation of free primary and secondary benzylamines using Pd<sup>II</sup> remains an outstanding challenge. Presented herein is a new strategy for constructing <i>ortho</i>-arylated primary and secondary benzylamines mediated by carbon dioxide (CO<sub>2</sub>). The use of CO<sub>2</sub> is critical to allowing this transformation to proceed under milder conditions than previously reported, and that are necessary to furnish free amine products that can be directly used or elaborated without the need for deprotection. In cases where diarylation is possible, a chelate effect is demonstrated to facilitate selective monoarylation.


1990 ◽  
Author(s):  
Isidore Last ◽  
Thomas F. George

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