The effect of central and planar chirality on the electrochemical and chiral sensing properties of ferrocenyl urea H-bonding receptors

2015 ◽  
Vol 44 (16) ◽  
pp. 7268-7275 ◽  
Author(s):  
Andrea Mulas ◽  
Yasmine Willener ◽  
James Carr-Smith ◽  
Kevin M. Joly ◽  
Louise Male ◽  
...  

Ferrocenyl urea receptors containing planar and central chirality electrochemically sense carboxylate anions via formation of H-bonded complexes.

2015 ◽  
Vol 13 (26) ◽  
pp. 7230-7235 ◽  
Author(s):  
N. Lokesh ◽  
S. L. Sachin ◽  
L. V. Narendra ◽  
K. Arun ◽  
N. Suryaprakash

The study reports chiral sensing properties of RNA nucleosides. A three component derivitazation protocol has been adopted to differentiate chiral amines. All RNA nucleosides exhibit chiral sensing property.


Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381 ◽  
Author(s):  
S Cosa ◽  
AM Viljoen ◽  
SK Chaudhary ◽  
W Chen

2013 ◽  
Vol 28 (6) ◽  
pp. 584-588 ◽  
Author(s):  
Shuang XU ◽  
Ying YANG ◽  
Hong-Yuan WU ◽  
Chao JIANG ◽  
Li-Qiang JING ◽  
...  

2020 ◽  
Vol 17 (6) ◽  
pp. 472-478
Author(s):  
Wei-tao Gong ◽  
Wei-dong Qu ◽  
Guiling Ning

Two pyridinium amide-based receptors L1 and L2 with a small difference of H-bond position of the amide have been synthesized and characterized. Interestingly, they exhibited a huge difference in sensing towards AcO- and H2PO4 -, respectively. Receptor L1 was found to be ‘naked-eye’ selective for AcO- anions, while receptor L2 showed clear fluorescence enhancement selective to H2PO4 - anion. The recognition ability has been established by fluorescence emission, UV-vis spectra, and 1HNMR titration.


Molecules ◽  
2019 ◽  
Vol 24 (23) ◽  
pp. 4399 ◽  
Author(s):  
Ibon Alkorta ◽  
José Elguero ◽  
Manuel Yáñez ◽  
Otilia Mó ◽  
M. Merced Montero-Campillo

Relativistic effects are found to be important for the estimation of NMR parameters in halogen-bonded complexes, mainly when they involve the heavier elements, iodine and astatine. A detailed study of 60 binary complexes formed between dihalogen molecules (XY with X, Y = F, Cl, Br, I and At) and four Lewis bases (NH3, H2O, PH3 and SH2) was carried out at the MP2/aug-cc-pVTZ/aug-cc-pVTZ-PP computational level to show the extent of these effects. The NMR parameters (shielding and nuclear quadrupolar coupling constants) were computed using the relativistic Hamiltonian ZORA and compared to the values obtained with a non-relativistic Hamiltonian. The results show a mixture of the importance of the relativistic corrections as both the size of the halogen atom and the proximity of this atom to the basic site of the Lewis base increase.


2003 ◽  
Vol 9 (10) ◽  
pp. 2239-2244 ◽  
Author(s):  
Bohumil Štíbr ◽  
Josef Holub ◽  
Mario Bakardjiev ◽  
Ivan Pavlík ◽  
Oleg L. Tok ◽  
...  
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