2021
DOI: 10.1016/j.porgcoat.2021.106417
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Recent advances of organogels: from fabrications and functions to applications

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Cited by 67 publications
(50 citation statements)
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“…Due to the possession of the pillar[5]arene cavity on the structural skeleton, P11 could form a complex with a neutral poly(ethylene glycol) (PEG) derivative with two ending subunits—alkylnitrile G4 ( Scheme 4 ) via donor–acceptor interactions. Particularly, this obtained host–guest inclusion P11 ⸧ G4 not only has the capacity for properly exfoliating and dispersing single-walled carbon nanotubes in organic solvents (600 μg mL −1 , Figure 2 ) as confirmed by 1 H NMR, Raman, UV–Vis–near-infrared (NIR) spectra, and thermogravimetric analysis (TGA), but also affords the preparation of pillar[5]arene-based polymer-carbon nanotube composite organogels [ 88 , 89 , 90 ] in 1,2-dichlorobenzene (40 wt %) via non-covalent interactions ( Figure 3 ) [ 85 ].…”
Section: Decoration Of Carbon Nanotube By Using Functional Pillar[n]a...mentioning
confidence: 99%
“…Due to the possession of the pillar[5]arene cavity on the structural skeleton, P11 could form a complex with a neutral poly(ethylene glycol) (PEG) derivative with two ending subunits—alkylnitrile G4 ( Scheme 4 ) via donor–acceptor interactions. Particularly, this obtained host–guest inclusion P11 ⸧ G4 not only has the capacity for properly exfoliating and dispersing single-walled carbon nanotubes in organic solvents (600 μg mL −1 , Figure 2 ) as confirmed by 1 H NMR, Raman, UV–Vis–near-infrared (NIR) spectra, and thermogravimetric analysis (TGA), but also affords the preparation of pillar[5]arene-based polymer-carbon nanotube composite organogels [ 88 , 89 , 90 ] in 1,2-dichlorobenzene (40 wt %) via non-covalent interactions ( Figure 3 ) [ 85 ].…”
Section: Decoration Of Carbon Nanotube By Using Functional Pillar[n]a...mentioning
confidence: 99%
“…The most dominating choices to generate supramolecular cross-linking are hydrogen bonding, 15 electrostatic interactions, 16 π interactions, 17 and host−guest mechanisms. 18,19 Macroscale cross-linked porous polymer networks can be classified by the nature of polymer chains in a way that a library of materials based on aqueous-air nature (i.e., hydrogels, 20,21 aerogels 22 ), organic nature (i.e., resins, 23 organogels 24 ), and silicon-based nature (i.e., (polydimethylsiloxane)s 25 ) exist. The porosity of aforementioned networks is identified via "swelling" and "solvent uptake" parameters.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Consequently, the development of materials with fouling-resistant properties that could eliminate the issue resulting from marine biofouling is feasible and urgently needed. Recently, many anti-fouling strategies of utilizing coating materials to prevent protein, cell, and fouling organism adhesion have been proposed, including (super)hydrophobic materials [ 3 , 4 ], bio-inspired antiadhesive micro/nanostructures [ 5 , 6 ], siloxane/fluorocarbon-based fouling release coatings [ 1 , 7 ], amphiphilic coatings [ 8 , 9 ], and polymer gels [ 10 , 11 , 12 , 13 , 14 ]. In particular, hydrogels, a soft and wet polymeric material, are significantly different from the dry and hard solid surfaces, which play crucial roles in the anti-fouling property due to the potential super wettability and surface lubricity [ 15 ].…”
Section: Introductionmentioning
confidence: 99%