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Journal articles on the topic 'Organosilica'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Mohd, Hanafi Ani, Maziati Akmal Mohd Hatta, and Raihan Othman. "Effect of Al Ions on Adsorption Efficiency of Mesoporous Organosilica for Water Treatment." Advanced Materials Research 415-417 (December 2011): 2024–31. http://dx.doi.org/10.4028/www.scientific.net/amr.415-417.2024.

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Porous organosilica is a promising material to be applied in water treatment due to high adsorption capacity of contaminants. Sol-gel method was used to fabricate mesoporous organosilioca from triblock copolymers, poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) as the template and tetraethylorthosilicate as silicate source. The organosilica is doped with Al powder and Al2SO3 in order to evaluate the effect of ions on their adsorption capacity. It was demonstrated that the adsorption capacity is proportional to Al concentration, and inversely proportional to porosity. Metallic compound doped in organosilica enhances the remediation process and optimize the water treatment process. Moreover, impregnation the samples into cellulosic sponge improves the adsorption efficiency by 25%.

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2

Asefa, Tewodros, and Zhimin Tao. "Mesoporous silica and organosilica materials — Review of their synthesis and organic functionalization." Canadian Journal of Chemistry 90, no. 12 (December 2012): 1015–31. http://dx.doi.org/10.1139/v2012-094.

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Mesoporous silica and organosilica materials are a class of nanostructured materials that have porous structures with tunable nanometer pores, large surface areas, high pore volumes, and, in some cases, well-ordered mesostructures. Furthermore, in the case of mesoporous organosilicas, the materials possess various types of organic functional groups. This review highlights the different synthetic methods developed for mesoporous silica and organosilica nanomaterials. The review also discusses the various synthetic strategies used to functionalize the surfaces of mesoporous silica materials and produce highly functionalized mesoporous materials. Rational design and synthetic methods developed to place judiciously chosen one or more than one type of functional group(s) on the surfaces of mesoporous silica materials and generate monofunctional and multifunctional mesoporous silica materials are also introduced. These organic functionalization methods have made possible the synthesis of organically functionalized mesoporous silicas and mesoporous organosilicas with various interesting properties and many potential applications in different areas, ranging from catalysis to drug delivery and biosensing.

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3

Nakamura, Michihiro. "Biomedical applications of organosilica nanoparticles toward theranostics." Nanotechnology Reviews 1, no. 6 (December 1, 2012): 469–91. http://dx.doi.org/10.1515/ntrev-2012-0005.

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AbstractNanoparticles for biomedical applications have several advantages as multifunctional agents. Among various types of nanoparticles for biomedical applications, silica nanoparticles have characteristic positioning due to their inherent property. The recent development of silica nanoparticles is creating a new trend in nanomedicine. A novel type of silica nanoparticle, organosilica nanoparticle, is both structurally and functionally different from the common (inorgano)silica nanoparticle. The organosilica nanoparticles are inherent organic-inorganic hybrid nanomaterials. The interior and exterior functionalities of organosilica nanoparticles are useful for their multifunctionalization. Biomedical applications of organosilica nanoparticles are leading to a wide range of nanomedical fields such as basic biomedical investigations and clinical applications. Multifunctionalizations peculiar to organosilica nanoparticles enable the creation of novel imaging systems and therapeutic applications. In this review, I will introduce differences between (inorgano)silica nanoparticles and organosilica nanoparticles, and then focus on biomedical applications of organosilica nanoparticles toward theranostics.

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4

Niu, Dechao, Yongsheng Li, and Jianlin Shi. "Silica/organosilica cross-linked block copolymer micelles: a versatile theranostic platform." Chemical Society Reviews 46, no. 3 (2017): 569–85. http://dx.doi.org/10.1039/c6cs00495d.

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Silica/organosilica cross-linked block copolymer micelles are a novel class of hybrid materials that combine the advantages of amphiphilic block copolymers and silica/organosilica cross-linking agents into one unit. This Tutorial Review summarizes the recent progress in the design, synthesis and biomedical applications of various silica/organosilica cross-linked block copolymer micelles.

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5

Poscher, Vanessa, and Yolanda Salinas. "Trends in Degradable Mesoporous Organosilica-Based Nanomaterials for Controlling Drug Delivery: A Mini Review." Materials 13, no. 17 (August 19, 2020): 3668. http://dx.doi.org/10.3390/ma13173668.

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The last few years of enhancing the design of hybrid mesoporous organosilica nanoparticleshas allowed their degradation under specific pathologic conditions, which finally is showing a lightin their potential use as drug delivery systems towards clinical trials. Nevertheless, the issueof controlling the degradation on-demand at cellular level still remains a major challenge, even if ithas lately been addressed through the incorporation of degradable organo-bridged alkoxysilanesinto the silica framework. On this basis, this mini review covers some of the most recent examplesof dierent degradable organosilica nanomaterials with potential application in nanomedicine,from degradable non-porous to mesoporous organosilica nanoparticles (MONs), functionalized withresponsive molecular gates, and also the very promising degradable periodic mesoporous organosilicamaterials (PMOs) only consisting of organosilica bridges.

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6

Zebardasti, Ali, Mohammad Dekamin, and Esmail Doustkhah. "The Isocyanurate-Carbamate-Bridged Hybrid Mesoporous Organosilica: An Exceptional Anchor for Pd Nanoparticles and a Unique Catalyst for Nitroaromatics Reduction." Catalysts 11, no. 5 (May 12, 2021): 621. http://dx.doi.org/10.3390/catal11050621.

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Hybridisation of mesoporous organosilicas (MO) to reinforce the surface capability in adsorption and stabilisation of noble metal nanoparticles is of great attention in generating/supporting noble metal within their matrices and transforming them into efficient heterogeneous catalysts. Here, we used a unique hybrid of organic-inorganic mesoporous silica in which pore profile pattern was similar to the well-known mesoporous silica, SBA-15 for catalysis. This hybrid mesoporous organosilica was further engaged as a support in the synthesis and stabilisation of Pd nanoparticles on its surface, and then, the obtained Pd-supported MO was employed as a heterogeneous green catalyst in the conversion of aqueous p-nitrophenol (PNP) to p-aminophenol (PAP) at room temperature with efficient recyclability.

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7

Ren and Tsuru. "Organosilica-Based Membranes in Gas and Liquid-Phase Separation." Membranes 9, no. 9 (August 22, 2019): 107. http://dx.doi.org/10.3390/membranes9090107.

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Organosilica membranes are a type of novel materials derived from organoalkoxysilane precursors. These membranes have tunable networks, functional properties and excellent hydrothermal stability that allow them to maintain high levels of separation performance for extend periods of time in either a gas-phase with steam or a liquid-phase under high temperature. These attributes make them outperform pure silica membranes. In this review, types of precursors, preparation method, and synthesis factors for the construction of organosilica membranes are covered. The effects that these factors exert on characteristics and performance of these membranes are also discussed. The incorporation of metals, alkoxysilanes, or other functional materials into organosilica membranes is an effective and simple way to improve their hydrothermal stability and achieve preferable chemical properties. These hybrid organosilica membranes have demonstrated effective performance in gas and liquid-phase separation.

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8

Jaroniec, Mietek. "Organosilica the conciliator." Nature 442, no. 7103 (August 2006): 638–40. http://dx.doi.org/10.1038/442638a.

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9

Knezevic, Nikola Z., Chiara Mauriello Jimenez, Martin Albino, Aleksandar Vukadinovic, Ana Mrakovic, Erzsebet Illes, Djordje Janackovic, Jean-Olivier Durand, Claudio Sangregorio, and Davide Peddis. "Synthesis and Characterization of Core-Shell Magnetic Mesoporous Silica and Organosilica Nanostructures." MRS Advances 2, no. 19-20 (2017): 1037–45. http://dx.doi.org/10.1557/adv.2017.69.

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ABSTRACTInitial results en route toward construction of complex magnetic core-shell silica and organosilica nanotheranostics are presented. Magnetite nanoparticles are synthesized by three different methods and embedded within mesoporous silica and organosilica frameworks by different surfactant-templated procedures to produce three types of core-shell nanoparticles. Magnetite nanoparticles (15 nm in diameter) are embedded within mesoporous silica nanoparticles to produce cell-like material with predominantly one magnetite nuclei-resembling core per nanoparticle, with final particle diameter of ca. 150 nm, specific surface area of 573 m2/g and hexagonally structured tubular pores (2.6 nm predominant diameter), extended throughout the volume of nanoparticles. Two forms of spherical core-shell nanoparticles composed of magnetite cores embedded within mesoporous organosilica shells are also obtained by employing ethylene and ethane bridged organobisalkoxysilane precursors. The obtained nanomaterials are characterized by high surface area (978 and 820 m2/g), tubular pore morphology (2 and 2.8 nm predominant pore diameters), different diameters (386 and 100-200 nm), in case of ethylene- and ethane-composed organosilica shells, respectively. Different degree of agglomeration of magnetite nanoparticles was also observed in the obtained materials, and in the case of utilization of surfactant-pre-stabilized magnetite nanoparticles for the syntheses, their uniform and non-agglomerated distribution within the shells was noted.

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10

Poscher, Vanessa, George S. Pappas, Oliver Brüggemann, Ian Teasdale, and Yolanda Salinas. "Hybrid Porous Microparticles Based on a Single Organosilica Cyclophosphazene Precursor." International Journal of Molecular Sciences 21, no. 22 (November 13, 2020): 8552. http://dx.doi.org/10.3390/ijms21228552.

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Porous organosilica microparticles consisting of silane-derived cyclophosphazene bridges were synthesized by a surfactant-mediated sol-gel process. Starting from the substitution of hexachlorocyclotriphosphazene with allylamine, two different precursors were obtained by anchoring three or six alkoxysilane units, via a thiol-ene photoaddition reaction. In both cases, spherical, microparticles (size average of ca. 1000 nm) with large pores were obtained, confirmed by both, scanning and transmission electron microscopy. Particles synthesized using the partially functionalized precursor containing free vinyl groups were further functionalized with a thiol-containing molecule. While most other reported mesoporous organosilica particles are essentially hybrids with tetraethyl orthosilicate (TEOS), a unique feature of these particles is that structural control is achieved by exclusively using organosilane precursors. This allows an increase in the proportion of the co-components and could springboard these novel phosphorus-containing organosilica microparticles for different areas of technology.

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11

Shvets, D., T. Denisova, and V. Strelko. "Carbon, natural and synthetic sorbents for decontamination of objects of ecosystems from pathogenic microflora." Open Chemistry 1, no. 2 (June 1, 2003): 178–91. http://dx.doi.org/10.2478/bf02479267.

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AbstractPhysico-chemical characteristics and sorption activity of carbon, organosilica sorbents and their modified forms towards proteins, possessing specific activity, and cholerae vibrio have been studied. It was found, that carbon materials modified by copper (II) effectively extracts cholerae vibrio (100%) and may be recommended for disinfection of drinking water. Sorption capacity of organosilica sorbents and their modified by copper (II) forms towards pathogenic microflora (E.coli, St.aureus, Ps.aeruginosa) depending on the composition of the sorbents, concentration of the modified reagent, pH of medium have been evaluated. The rows of the increase of sorption of pathogenic microorganisms by synthetic sorbents in water-salt solutions were established: Al(III)<Zn(II)<Cu (II). It was shown that inhibiting effect of modified synthetic organosilica and natural sorbents towards such pathogenic microorganisms as E-coli, St.aureus Ps.aeruginosa and fungus Bacillus pyocyaneus accordingly is equal 80–98%.

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12

Guo, Meng, and Masakoto Kanezashi. "Recent Progress in a Membrane-Based Technique for Propylene/Propane Separation." Membranes 11, no. 5 (April 23, 2021): 310. http://dx.doi.org/10.3390/membranes11050310.

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The similar physico-chemical properties of propylene and propane molecules have made the separation process of propylene/propane challenging. Membrane separation techniques show substantial prospects in propylene/propane separation due to their low energy consumption and investment costs, and they have been proposed to replace or to be combined with the conventional cryogenic distillation process. Over the past decade, organosilica membranes have attracted considerable attention due to their significant features, such as their good molecular sieving properties and high hydrothermal stability. In the present review, holistic insight is provided to summarize the recent progress in propylene/propane separation using polymeric, inorganic, and hybrid membranes, and a particular inspection of organosilica membranes is conducted. The importance of the pore subnano-environment of organosilica membranes is highlighted, and future directions and perspectives for propylene/propane separation are also provided.

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13

Seet, Katrina Y. T., Robert Vogel, Timo A. Nieminen, Gregor Knöner, Halina Rubinsztein-Dunlop, Matt Trau, and Andrei V. Zvyagin. "Refractometry of organosilica microspheres." Applied Optics 46, no. 9 (March 1, 2007): 1554. http://dx.doi.org/10.1364/ao.46.001554.

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14

Lofgreen, Jennifer E., Igor L. Moudrakovski, and Geoffrey A. Ozin. "Molecularly Imprinted Mesoporous Organosilica." ACS Nano 5, no. 3 (February 16, 2011): 2277–87. http://dx.doi.org/10.1021/nn1035697.

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15

Mohanty, Paritosh, and Kai Landskron. "Periodic Mesoporous Organosilica Nanorice." Nanoscale Research Letters 4, no. 2 (November 22, 2008): 169–72. http://dx.doi.org/10.1007/s11671-008-9219-0.

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16

Croutxé-Barghorn, Céline, Abraham Chemtob, Lingli Ni, and Irena Deroche. "Photoinduced nanostructured organosilica hybrids." Polymer International 66, no. 5 (December 26, 2016): 640–46. http://dx.doi.org/10.1002/pi.5300.

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17

Teng, Zhaogang, Wei Li, Yuxia Tang, Ahmed Elzatahry, Guangming Lu, and Dongyuan Zhao. "Organosilica: Mesoporous Organosilica Hollow Nanoparticles: Synthesis and Applications (Adv. Mater. 38/2019)." Advanced Materials 31, no. 38 (September 2019): 1970273. http://dx.doi.org/10.1002/adma.201970273.

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18

Ferré, M., R. Pleixats, M. Wong Chi Man, and X. Cattoën. "Recyclable organocatalysts based on hybrid silicas." Green Chemistry 18, no. 4 (2016): 881–922. http://dx.doi.org/10.1039/c5gc02579f.

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19

Doustkhah, Esmail, Sadegh Rostamnia, Masataka Imura, Yusuke Ide, Shiva Mohammadi, Christopher J. T. Hyland, Jungmok You, Nao Tsunoji, Behzad Zeynizadeh, and Yusuke Yamauchi. "Thiourea bridged periodic mesoporous organosilica with ultra-small Pd nanoparticles for coupling reactions." RSC Advances 7, no. 89 (2017): 56306–10. http://dx.doi.org/10.1039/c7ra11711f.

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20

Liu, Wenfei, Ying Tian, Yunlei Zhang, Kai Liu, Shuang Zhao, Junjie Zhang, Yunyan Su, et al. "Timely coordinated phototherapy mediated by mesoporous organosilica coated triangular gold nanoprisms." Journal of Materials Chemistry B 6, no. 23 (2018): 3865–75. http://dx.doi.org/10.1039/c8tb00541a.

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21

Haghighat, Mahdieh, Farhad Shirini, and Mostafa Golshekan. "Synthesis of Tetrahydrobenzo[b]pyran and Pyrano[2, 3-d]pyrimidinone Derivatives Using Fe3O4@Ph-PMO-NaHSO4 as a New Magnetically Separable Nanocatalyst." Journal of Nanoscience and Nanotechnology 19, no. 6 (June 1, 2019): 3447–58. http://dx.doi.org/10.1166/jnn.2019.16032.

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Immobilized NaHSO4 on core/shell phenylene bridged periodic mesoporous organosilica magnetic nanoparticles (Fe3O4@Ph-PMO-NaHSO4) as a new acidic magnetically separable nanocatalyst was successfully prepared in three steps: (i) preparation of Fe3O4 nanoparticles by a precipitation method, (ii) synthesis of an organic–inorganic periodic mesoporous organosilica structure with phenyl groups on the surface of Fe3O4 magnetic nanoparticles (MNPs) and (iii) finally adsorption of NaHSO4 on periodic mesoporous organosilica (PMO) network. The prepared organic–inorganic magnetic reagent was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), transmission electron microscopy (TEM), N2 adsorption–desorption and energy-dispersive X-ray (EDX) techniques. Finally, it was used as a reusable and new catalyst to promote the synthesis of tetrahydrobenzo[b]pyran and pyrano[2,3-d]pyrimidinone derivatives as important biologically active compounds. Eco-friendly protocol, high yields, short reaction times and easy and quick isolation of the products are the main advantages of this procedure.

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22

Denisova, T. I., and D. I. Shvetz. "Modified Organosilica Adsorbents with Bactericidal Properties." Adsorption Science & Technology 20, no. 3 (April 2002): 285–93. http://dx.doi.org/10.1260/026361702760254469.

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The method of mathematical planning of experiments has been used to determine the optimal conditions for the formation of a two-component organosilica with various compositions modified by metal ions (CuII, ZnII) sorbed from their water–ammonia solutions. Through this method, modified forms of silico-polymethylsiloxanes (SG-PMS) containing 1–30 mg/g CuII ion [SG-PMS(Cu)] and 3–40 mg/g ZnII ion [SG-PMS(Zn)] were synthesized and their adsorption/structural characteristics established. The sorptive capacity of the organosilica sorbents and their modified forms towards pathogenic microflora ( E. coli, S. aureus, P. aeruginosa), which depend on the concentration of the modified component, the pH of the medium and the sorptional composition, has been evaluated. It was found that the sorption levels of microorganisms increased in the following sorbent-modified range: 30:70 wt% SG-PMS(Al) < 50:50 wt% SG-PMS(Zn) < 50:50 wt% SG-PMS(Cu) and attained values in the range of 81–98% for metal-containing forms depending on the pH of the medium and the nature of the microorganisms. Copper-containing forms of organosilica exhibited an inhibiting effect towards pathogenic microorganisms even at CuII ion-containing contents of only 1 mg/g.

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23

Tao, Jun, Kun Chen, Xiaodan Su, Lili Ren, Junjie Zhang, Lei Bao, Heng Dong, Guangming Lu, Zhaogang Teng, and Lianhui Wang. "Virus-mimicking mesoporous organosilica nanocapsules with soft framework and rough surface for enhanced cellular uptake and tumor penetration." Biomaterials Science 8, no. 8 (2020): 2227–33. http://dx.doi.org/10.1039/c9bm01559k.

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24

Rahmani, Saher, Arnaud Chaix, Dina Aggad, Phuong Hoang, Basem Moosa, Marcel Garcia, Magali Gary-Bobo, et al. "Degradable gold core–mesoporous organosilica shell nanoparticles for two-photon imaging and gemcitabine monophosphate delivery." Mol. Syst. Des. Eng. 2, no. 4 (2017): 380–83. http://dx.doi.org/10.1039/c7me00058h.

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25

Mauriello-Jimenez, Chiara, Jonas Croissant, Marie Maynadier, Xavier Cattoën, Michel Wong Chi Man, Julien Vergnaud, Vincent Chaleix, et al. "Porphyrin-functionalized mesoporous organosilica nanoparticles for two-photon imaging of cancer cells and drug delivery." Journal of Materials Chemistry B 3, no. 18 (2015): 3681–84. http://dx.doi.org/10.1039/c5tb00315f.

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26

Yin, Quanyi, Shuhua Tu, Min Chen, and Limin Wu. "Novel Polymeric Organosilica Precursor and Emulsion Stabilizer: Toward Highly Elastic Hollow Organosilica Nanospheres." Langmuir 35, no. 35 (August 9, 2019): 11524–32. http://dx.doi.org/10.1021/acs.langmuir.9b02062.

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27

Choi, Seokwon, Youngkyoo Kim, Il Kim, and Chang-Sik Ha. "Effect of organosilica isomers on the interfacial interaction in polyimide/aromatic organosilica hybrids." Journal of Applied Polymer Science 103, no. 4 (2006): 2507–13. http://dx.doi.org/10.1002/app.24864.

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28

Wahab, M. Abdul, S. W. Chu, C. Anand, and Chang-Sik Ha. "Synthesis and Characterization of Multifunctional Periodic Mesoporous Organosilica from Diureidophenylene Bridged Organosilica Precursor." Journal of Nanoscience and Nanotechnology 12, no. 6 (June 1, 2012): 4531–39. http://dx.doi.org/10.1166/jnn.2012.6215.

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29

Luka, M., and S. Polarz. "Wiring functional groups in mesoporous organosilica materials." Journal of Materials Chemistry C 3, no. 10 (2015): 2195–203. http://dx.doi.org/10.1039/c4tc02746a.

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30

Taubert, Andreas, Ruben Löbbicke, Barbara Kirchner, and Fabrice Leroux. "First examples of organosilica-based ionogels: synthesis and electrochemical behavior." Beilstein Journal of Nanotechnology 8 (March 29, 2017): 736–51. http://dx.doi.org/10.3762/bjnano.8.77.

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The article describes the synthesis and properties of new ionogels for ion transport. A new preparation process using an organic linker, bis(3-(trimethoxysilyl)propyl)amine (BTMSPA), yields stable organosilica matrix materials. The second ionogel component, the ionic liquid 1-methyl-3-(4-sulfobutyl)imidazolium 4-methylbenzenesulfonate, [BmimSO3H][PTS], can easily be prepared with near-quantitative yields. [BmimSO3H][PTS] is the proton conducting species in the ionogel. By combining the stable organosilica matrix with the sulfonated ionic liquid, mechanically stable, and highly conductive ionogels with application potential in sensors or fuel cells can be prepared.

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31

Wu, Dan, Yuchuan Liu, Yue Wu, Bin Tan, and Zailai Xie. "Microporous carbons derived from organosilica-containing carbon dots with outstanding supercapacitance." Dalton Transactions 47, no. 17 (2018): 5961–67. http://dx.doi.org/10.1039/c8dt00484f.

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32

Yang, Lingang, Lingzhi Wang, Chuanfeng Cui, Juying Lei, and Jinlong Zhang. "Stöber strategy for synthesizing multifluorescent organosilica nanocrystals." Chemical Communications 52, no. 36 (2016): 6154–57. http://dx.doi.org/10.1039/c6cc01917j.

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33

López, María I., Dolores Esquivel, César Jiménez-Sanchidrián, Pascal Van Der Voort, and Francisco J. Romero-Salguero. "Thiol-Functionalized Ethylene Periodic Mesoporous Organosilica as an Efficient Scavenger for Palladium: Confirming the Homogeneous Character of the Suzuki Reaction." Materials 13, no. 3 (January 30, 2020): 623. http://dx.doi.org/10.3390/ma13030623.

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This work describes the synthesis of thiol-functionalized periodic mesoporous organosilicas (PMOs) prepared using the precursor 1-thiol-1,2-bis(triethoxysilyl)ethane, alone or mixed with 1,2-bis(triethoxysilyl)ethane. The thiol groups incorporated into the structure were found to be efficient for palladium binding. This has allowed these materials to be used as catalysts in the Suzuki cross-coupling reaction of bromobenzene and phenylboronic acid. Their performance has been compared to palladium-supported periodic mesoporous (organo)silicas and important differences have been observed between them. The use of different heterogeneity tests, such as hot filtration test and poisoning experiments, has provided a deep insight into the reaction mechanism and has confirmed that the reaction occurs in the homogeneous phase following a “release and catch” mechanism. Furthermore, the thiol-functionalized periodic mesoporous organosilica, synthesized using only 1-thiol-1,2-bis(triethoxysilyl)ethane as a precursor, has proven to be an efficient palladium scavenger.

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34

Kalantari, Mohammad, Meihua Yu, Manasi Jambhrunkar, Yang Liu, Yannan Yang, Xiaodan Huang, and Chengzhong Yu. "Designed synthesis of organosilica nanoparticles for enzymatic biodiesel production." Materials Chemistry Frontiers 2, no. 7 (2018): 1334–42. http://dx.doi.org/10.1039/c8qm00078f.

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35

Dang, Meng, Wei Li, Yuanyi Zheng, Xiaodan Su, Xiaobo Ma, Yunlei Zhang, Qianqian Ni, et al. "Mesoporous organosilica nanoparticles with large radial pores via an assembly-reconstruction process in bi-phase." Journal of Materials Chemistry B 5, no. 14 (2017): 2625–34. http://dx.doi.org/10.1039/c6tb03327j.

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36

Wahab, Mohammad A., and Jorge N. Beltramini. "Recent advances in hybrid periodic mesostructured organosilica materials: opportunities from fundamental to biomedical applications." RSC Advances 5, no. 96 (2015): 79129–51. http://dx.doi.org/10.1039/c5ra10062c.

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37

Wu, Datong, Wensheng Tan, Hongda Li, Zhangchen Lei, Linhong Deng, and Yong Kong. "A facile route to prepare functional mesoporous organosilica spheres with electroactive units for chiral recognition of amino acids." Analyst 144, no. 2 (2019): 543–49. http://dx.doi.org/10.1039/c8an01519h.

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Kalantari, Mohammad, Yang Liu, Ekaterina Strounina, Yannan Yang, Hao Song, and Chengzhong Yu. "Superhydrophobic dendritic mesoporous organosilica nano-particles with ultrahigh-content of gradient organic moieties." Journal of Materials Chemistry A 6, no. 36 (2018): 17579–86. http://dx.doi.org/10.1039/c8ta06268d.

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39

Dral, A. Petra, Kristianne Tempelman, Emiel J. Kappert, Louis Winnubst, Nieck E. Benes, and Johan E. ten Elshof. "Long-term flexibility-based structural evolution and condensation in microporous organosilica membranes for gas separation." Journal of Materials Chemistry A 5, no. 3 (2017): 1268–81. http://dx.doi.org/10.1039/c6ta09559c.

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40

Mirbagheri, Reza, Dawood Elhamifar, and Shaaker Hajati. "Ru-containing magnetic yolk–shell structured nanocomposite: a powerful, recoverable and highly durable nanocatalyst." RSC Advances 11, no. 17 (2021): 10243–52. http://dx.doi.org/10.1039/d0ra10304g.

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41

Mizoshita, Norihiro, Masamichi Ikai, Takao Tani, and Shinji Inagaki. "Hole-Transporting Periodic Mesostructured Organosilica." Journal of the American Chemical Society 131, no. 40 (October 14, 2009): 14225–27. http://dx.doi.org/10.1021/ja9050263.

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42

Dickson, Steven E., and Cathleen M. Crudden. "Transformable periodic mesoporous organosilica materials." Chemical Communications 46, no. 12 (2010): 2100. http://dx.doi.org/10.1039/b924570g.

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Wang, Lin, M. Carmen Estévez, Meghan O'Donoghu, and Weihong Tan. "Fluorophore-Free Luminescent Organosilica Nanoparticles." Langmuir 24, no. 5 (March 2008): 1635–39. http://dx.doi.org/10.1021/la703392m.

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Attia, Mohamed F., Maria I. Swasy, Mohamed Ateia, Frank Alexis, and Daniel C. Whitehead. "Periodic mesoporous organosilica nanomaterials for rapid capture of VOCs." Chemical Communications 56, no. 4 (2020): 607–10. http://dx.doi.org/10.1039/c9cc09024j.

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Song, Huating, Yibin Wei, and Hong Qi. "Tailoring pore structures to improve the permselectivity of organosilica membranes by tuning calcination parameters." Journal of Materials Chemistry A 5, no. 47 (2017): 24657–66. http://dx.doi.org/10.1039/c7ta07117e.

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Moorthy, Madhappan Santha, Hyun-Jin Song, Jae-Ho Bae, Sun-Hee Kim, and Chang-Sik Ha. "Red fluorescent hybrid mesoporous organosilicas for simultaneous cell imaging and anticancer drug delivery." RSC Adv. 4, no. 82 (2014): 43342–45. http://dx.doi.org/10.1039/c4ra08204d.

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Wang, Xia, Indre Thiel, Alexey Fedorov, Christophe Copéret, Victor Mougel, and Marc Fontecave. "Site-isolated manganese carbonyl on bipyridine-functionalities of periodic mesoporous organosilicas: efficient CO2 photoreduction and detection of key reaction intermediates." Chemical Science 8, no. 12 (2017): 8204–13. http://dx.doi.org/10.1039/c7sc03512h.

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Knežević, Nikola Ž., and Goran N. Kaluđerović. "Silicon-based nanotheranostics." Nanoscale 9, no. 35 (2017): 12821–29. http://dx.doi.org/10.1039/c7nr04445c.

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Jana, Avijit, John Mondal, Parijat Borah, Sujan Mondal, Asim Bhaumik, and Yanli Zhao. "Ruthenium bipyridyl tethered porous organosilica: a versatile, durable and reusable heterogeneous photocatalyst." Chemical Communications 51, no. 53 (2015): 10746–49. http://dx.doi.org/10.1039/c5cc03067f.

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Shan, Bing-Qian, Jun-Ling Xing, Tai-Qun Yang, Bo Peng, Pan Hao, Yu-Xin Zong, Xin-Qing Chen, Qing-Song Xue, Kun Zhang, and Peng Wu. "One-pot co-condensation strategy for dendritic mesoporous organosilica nanospheres with fine size and morphology control." CrystEngComm 21, no. 27 (2019): 4030–35. http://dx.doi.org/10.1039/c9ce00593e.

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