Redox responsive supramolecular amphiphiles based on reversible charge transfer interactions

2009 ◽  
pp. 5380 ◽  
Author(s):  
Chao Wang ◽  
Yinsheng Guo ◽  
Yapei Wang ◽  
Huaping Xu ◽  
Xi Zhang
2018 ◽  
Vol 54 (23) ◽  
pp. 2922-2925 ◽  
Author(s):  
Dan Wu ◽  
Jie Shen ◽  
Hongzhen Bai ◽  
Guocan Yu

Two supramolecular amphiphiles are fabricated through directional charge-transfer interactions, which self-assemble into nanofibers and nanoribbons. Due to the existence of galactose on their surface, these self-assemblies act as a cell glue to agglutinate E. coli, benefiting from multivalent interactions.


2009 ◽  
Vol 121 (47) ◽  
pp. 9124-9127 ◽  
Author(s):  
Chao Wang ◽  
Yinsheng Guo ◽  
Yapei Wang ◽  
Huaping Xu ◽  
Ruji Wang ◽  
...  

2015 ◽  
Vol 3 (8) ◽  
pp. 1218-1227 ◽  
Author(s):  
Feng Liu ◽  
Yufei Ma ◽  
Lei Xu ◽  
Lichao Liu ◽  
Weian Zhang

A supramolecular photosensitizer delivery system has been established through the self-assembly of supramolecular amphiphiles constructed by the host–guest interaction between poly(ethylene glycol)-β-cyclodextrin (PEG-β-CD) and adamantane-terminated porphyrin derivatives bearing a disulfide bond (TPPC6-SS-Ada).


2002 ◽  
Vol 114 (24) ◽  
pp. 4807-4807 ◽  
Author(s):  
Young Jin Jeon ◽  
Parimal K. Bharadwaj ◽  
SooWhan Choi ◽  
Jae Wook Lee ◽  
Kimoon Kim

2016 ◽  
Vol 7 (19) ◽  
pp. 3268-3276 ◽  
Author(s):  
Ye Chen ◽  
Leilei Rui ◽  
Lichao Liu ◽  
Weian Zhang

Supramolecular amphiphiles based on a pillar[5]arene with enhanced photodynamic therapy have been fabricated.


2005 ◽  
Vol 70 (11) ◽  
pp. 1891-1908 ◽  
Author(s):  
František Hartl ◽  
Sandrine Vernier ◽  
Peter Belser

Redox-controlled luminescence quenching is presented for a new Ru(II)-bipyridine complex [Ru(bpy)2(1)]2+ where ligand 1 is an anthra[1,10]phenanthrolinequinone. The complex emits from a short-lived metal-to-ligand charge transfer, 3MLCT state (τ = 5.5 ns in deaerated acetonitrile) with a low luminescence quantum yield (5 × 10-4). The emission intensity becomes significantly enhanced when the switchable anthraquinone unit is reduced to corresponding hydroquinone. On the contrary, chemical one-electron reduction of the anthraquinone moiety to semiquinone in aprotic tetrahydrofuran results in total quenching of the emission.


2002 ◽  
Vol 41 (24) ◽  
pp. 4612-4612 ◽  
Author(s):  
Young Jin Jeon ◽  
Parimal K. Bharadwaj ◽  
SooWhan Choi ◽  
Jae Wook Lee ◽  
Kimoon Kim

Author(s):  
J. Taft∅

It is well known that for reflections corresponding to large interplanar spacings (i.e., sin θ/λ small), the electron scattering amplitude, f, is sensitive to the ionicity and to the charge distribution around the atoms. We have used this in order to obtain information about the charge distribution in FeTi, which is a candidate for storage of hydrogen. Our goal is to study the changes in electron distribution in the presence of hydrogen, and also the ionicity of hydrogen in metals, but so far our study has been limited to pure FeTi. FeTi has the CsCl structure and thus Fe and Ti scatter with a phase difference of π into the 100-ref lections. Because Fe (Z = 26) is higher in the periodic system than Ti (Z = 22), an immediate “guess” would be that Fe has a larger scattering amplitude than Ti. However, relativistic Hartree-Fock calculations show that the opposite is the case for the 100-reflection. An explanation for this may be sought in the stronger localization of the d-electrons of the first row transition elements when moving to the right in the periodic table. The tabulated difference between fTi (100) and ffe (100) is small, however, and based on the values of the scattering amplitude for isolated atoms, the kinematical intensity of the 100-reflection is only 5.10-4 of the intensity of the 200-reflection.


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