ChemInform Abstract: Efficient Visible Light Photoresponse Following Surface Complexation of Titanium Dioxide with Transition Metal Cyanides.

ChemInform ◽  
1989 ◽  
Vol 20 (17) ◽  
Author(s):  
E. VRACHNOU ◽  
M. GRAETZEL ◽  
A. J. MCEVOY
Author(s):  
Arumugavel Murugan ◽  
Venkata Nagarjuna Babu ◽  
Nagaraj Sabarinathan ◽  
Sharada Duddu. S

Here we report a visible-light-promoted metal-free regioselective C3-H trifluoromehtylation reaction that proceeds via radical mechanism and which supported by control experiments. The combination of photoredox catalysis and hypervalent iodine reagent provides a practical approach for the present trifluoromethylation reaction and synthesis of a library of trifluoromethylated indazoles.


2021 ◽  
Vol 19 (16) ◽  
pp. 3735-3742
Author(s):  
Se Hyun Kim ◽  
Ju Hyeon An ◽  
Jun Hee Lee

Here, we provide an operationally simple protocol for the highly chemoselective deoxygenation of various functionalized N-heterocyclic N-oxides under visible light-mediated photoredox conditions with Na2-eosin Y as an organophotocatalyst.


2021 ◽  
Vol 57 (23) ◽  
pp. 2923-2926
Author(s):  
Yuanyuan Guo ◽  
Li Jiang ◽  
Ari Paavo Seitsonen ◽  
Bodong Zhang ◽  
Joachim Reichert ◽  
...  

Discriminatory on-surface complexation by the natural peptide CsA: up to two K atoms within its macrocycle, Co to residue 9 and the macrocycle, Fe non-selectively.


1982 ◽  
Vol 60 (17) ◽  
pp. 2194-2197 ◽  
Author(s):  
Roderick E. Wasylishen

Carbon-13/carbon-12 isotope-induced 15N chemical shifts of 0.06 to 0.10 ppm have been observed for the cyanide ion and several transition metal cyanides. In each case, the 15N resonance of the 13C labelled isotopomers is to high field of that in the corresponding carbon-12 species. The sensitivity of the 15N and 13C shielding constants in the cyanide ion to small changes in the CN bond length are evaluated using the theoretical formulation of Jameson: (∂σ(15N)/∂r)e = −872 ± 160 ppm/Å and (∂σ(13C)/∂r)e = −473 ± 90 ppm/Å. Nitrogen-15 chemical shifts in the metal complexes exhibit basically the same behaviour as do the 13C chemical shifts in these same complexes.


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