Periodic mesoporous silica having covalently attached tris(bipyridine)ruthenium complex: synthesis, photovoltaic and electrochemiluminescent properties

2007 ◽  
Vol 17 (22) ◽  
pp. 2336-2343 ◽  
Author(s):  
Josep Font ◽  
Pedro de March ◽  
Félix Busqué ◽  
Eva Casas ◽  
Miriam Benitez ◽  
...  
2016 ◽  
Vol 45 (45) ◽  
pp. 18147-18155 ◽  
Author(s):  
Gaochao Lv ◽  
Ling Qiu ◽  
Guiqing Liu ◽  
Wei Wang ◽  
Ke Li ◽  
...  

A pH sensitive mesoporous silica nanocarrier, RuNHC@MSNs-CTS-Biotin (CTS = chitosan), is developed for the targeted delivery and controlled release of a ruthenium(ii) N-heterocyclic carbene (RuNHC) complex.


2020 ◽  
Vol 124 (39) ◽  
pp. 21502-21511
Author(s):  
Tatsuya Watase ◽  
Minoru Sohmiya ◽  
Zhujun Zhang ◽  
Yasuhiro Kobori ◽  
Takashi Tachikawa

Nanoscale ◽  
2020 ◽  
Vol 12 (17) ◽  
pp. 9517-9523 ◽  
Author(s):  
Huizhen Fan ◽  
Yu Fan ◽  
Wenna Du ◽  
Rui Cai ◽  
Xinshuang Gao ◽  
...  

ICG forms aggregates in positively charged mesoporous silica, which show an enhanced type I photoreaction pathway.


2003 ◽  
Vol 775 ◽  
Author(s):  
G.V.Rama Rao ◽  
Qiang Fu ◽  
Linnea K. Ista ◽  
Huifang Xu ◽  
S. Balamurugan ◽  
...  

AbstractThis study details development of hybrid mesoporous materials in which molecular transport through mesopores can be precisely controlled and reversibly modulated. Mesoporous silica materials formed by surfactant templating were modified by surface initiated atom transfer radical polymerization of poly(N-isopropyl acrylamide) (PNIPAAm) a stimuli responsive polymer (SRP) within the porous network. Thermo gravimetric analysis and FTIR spectroscopy were used to confirm the presence of PNIPAAm on the silica surface. Nitrogen porosimetry, transmission electron microscopy and X-ray diffraction analyses confirmed that polymerization occurred uniformly within the porous network. Uptake and release of fluorescent dyes from the particles was monitored by spectrofluorimetry and scanning laser confocal microscopy. Results suggest that the presence of PNIPAAm, a SRP, in the porous network can be used to modulate the transport of aqueous solutes. At low temperature, (e.g., room temperature) the PNIPAAm is hydrated and extended and inhibits transport of analytes; at higher temperatures (e.g., 50°C) it is hydrophobic and is collapsed within the pore network, thus allowing solute diffusion into or out of the mesoporous silica. The transition form hydrophilic to hydrophobic state on polymer grafted mesoporous membranes was determined by contact angle measurements. This work has implications for the development of materials for the selective control of transport of molecular solutes in a variety of applications.


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