nach oben

Erschienen in:

2018 | OriginalPaper | Buchkapitel

2. Supramolecular Gels

verfasst von : Jianyong Zhang, Ya Hu, Yongguang Li

Erschienen in: Gel Chemistry

Verlag: Springer Singapore

Einloggen

Aktivieren Sie unsere intelligente Suche, um passende Fachinhalte oder Patente zu finden.

search-config

KI-gestützte Suche

Aus

Abstract

Supramolecular gels constructed by the assembly of small molecules have been extensively investigated. The gels bearing functional groups also exhibit intelligent and potential applications in the fields of tissue engineering and wound healing, drug delivery, templating or transcribing self-assembly morphology, molecular electronics, sensing and so forth. Due to various kinds of weak non-covalent interactions, abundant architectures are constructed and are smart to the external stimuli, such as temperature, light, mechanical stress, chemical, pH value. Therefore, supramolecular gels are sorted and stated according to different stimuli in this chapter.

Sie haben noch keine Lizenz? Dann Informieren Sie sich jetzt über unsere Produkte:

Springer Professional "Wirtschaft+Technik"

Online-Abonnement

Mit Springer Professional "Wirtschaft+Technik" erhalten Sie Zugriff auf:

über 102.000 Bücher
über 537 Zeitschriften

aus folgenden Fachgebieten:

Automobil + Motoren
Bauwesen + Immobilien
Business IT + Informatik
Elektrotechnik + Elektronik
Energie + Nachhaltigkeit
Finance + Banking
Management + Führung
Marketing + Vertrieb
Maschinenbau + Werkstoffe
Versicherung + Risiko

Jetzt Wissensvorsprung sichern!

Jetzt informieren

Springer Professional "Technik"

Online-Abonnement

Mit Springer Professional "Technik" erhalten Sie Zugriff auf:

über 67.000 Bücher
über 390 Zeitschriften

aus folgenden Fachgebieten:

Automobil + Motoren
Bauwesen + Immobilien
Business IT + Informatik
Elektrotechnik + Elektronik
Energie + Nachhaltigkeit
Maschinenbau + Werkstoffe

Jetzt Wissensvorsprung sichern!

Jetzt informieren

Vorheriges Kapitel Introduction

Nächstes Kapitel Metal–Organic Gels

Harada A, Kobayashi R, Takashima Y, Hashidzume A, Yamaguchi H (2011) Macroscopic self-assembly through molecular recognition. Nat Chem 3:34CrossRef

Park T, Zimmerman SC (2006) Formation of a miscible supramolecular polymer blend through self-assembly mediated by a quadruply hydrogen-bonded heterocomplex. J Am Chem Soc 128:11582CrossRef

Shirakawa M, Fujita N, Shinkai S (2003) [60]Fullerene-motivated organogel formation in a porphyrin derivative bearing programmed hydrogen-bonding sites. J Am Chem Soc 125:9902CrossRef

Dastidar P (2008) Supramolecular gelling agents: can they be designed? Chem Soc Rev 37:2699CrossRef

de Jong JDD, Feringa BL (2006) In Molecular gels, materials with self-assembled fibrillar networks. Springer, The Netherlands

Puigmartí-Luis J, Laukhin V, Pérez del Pino Á, Vidal-Gancedo J, Rovira C, Laukhina E, Amabilino DB (2007) Supramolecular conducting nanowires from organogels. Angew Chem Int Ed 46:238CrossRef

Yang Z, Ho P-L, Liang G, Chow KH, Wang Q, Cao Y, Guo Z, Xu B (2007) Using β-lactamase to trigger supramolecular hydrogelation. J Am Chem Soc 129:266CrossRef

Hirst AR, Escuder B, Miravet JF, Smith DK (2008) High-tech applications of self-assembling supramolecular nanostructured gel-phase materials: from regenerative medicine to electronic devices. Angew Chem Int Ed 47:8002CrossRef

Yu G, Yan X, Han C, Huang F (2013) Characterization of supramolecular gels. Chem Soc Rev 42:6697CrossRef

10.

Pal A, Dey J (2013) L-cysteine-derived ambidextrous gelators of aromatic solvents and ethanol/water mixtures. Langmuir 29:2120CrossRef

11.

Caplar V, Frkanec L, Sijakovic Vujicic N, Zinic M (2010) Positionally isomeric organic gelators: structure-gelation study, racemic versus enantiomeric gelators, and solvation effects. Chem Eur J 16:3066CrossRef

12.

Abraham S, Lan Y, Lam RS, Grahame DA, Kim JJ, Weiss RG, Rogers MA (2012) Influence of positional isomers on the macroscale and nanoscale architectures of aggregates of racemic hydroxyoctadecanoic acids in their molecular gel, dispersion, and solid states. Langmuir 28:4955CrossRef

13.

Piepenbrock MOM, Lloyd GO, Clarke N, Steed JW (2008) Gelation is crucially dependent on functional group orientation and may be tuned by anion binding. Chem Commun 2644

14.

Nakagawa T, Amakatsu M, Munenobu K, Fujii H, Yamanaka M (2013) Effect of optical purity of C3-symmetric chiral tris-ureas on supramolecular gel formation. Chem Lett 42:229CrossRef

15.

Grahame DAS, Olauson C, Lam RSH, Pedersen T, Borondics F, Abraham S, Weiss RG, Rogers MA (2011) Influence of chirality on the modes of self-assembly of 12-hydroxystearic acid in molecular gels of mineral oil. Soft Matter 7:7359CrossRef

16.

Kuroiwa K, Shibata T, Takada A, Nemoto N, Kimizuka N (2004) Heat-set gel-like networks of lipophilic Co(II) triazole complexes in organic media and their thermochromic structural transitions. J Am Chem Soc 126:2016CrossRef

17.

Peterca M, Imam MR, Ahn CH, Balagurusamy VS, Wilson DA, Rosen BM, Percec V (2011) Transfer, amplification, and inversion of helical chirality mediated by concerted interactions of C3-supramolecular dendrimers. J Am Chem Soc 133:2311CrossRef

18.

Kasha M (1963) Energy transfer mechanisms and the molecular exciton model for molecular aggregates. Radiat Res 20:55

19.

Yamane S, Sagara Y, Kato T (2013) Steric effects on excimer formation for photoluminescent smectic liquid-crystalline materials. Chem Commun 49:3839

20.

Das A, Molla MR, Maity B, Koley D, Ghosh S (2012) Hydrogen-bonding induced alternate stacking of donor (D) and acceptor (A) chromophores and their supramolecular switching to segregated states. Chemistry 18:9849CrossRef

21.

Bowen EJ, Sahu J (1959) The effect of temperature on fluorescence of solutions. J Phys Chem 63:4CrossRef

22.

Praveen VK, George SJ, Varghese R, Vijayakumar C, Ajayaghosh A (2006) Self-assembled π-nanotapes as donor scaffolds for selective and thermally gated fluorescence resonance energy transfer (FRET). J Am Chem Soc 128:7542CrossRef

23.

Zhao Z, Lam JWY, Tang BZ (2013) Self-assembly of organic luminophores with gelation-enhanced emission characteristics. Soft Matter 9:4564CrossRef

24.

Hong Y, Lam JWY, Tang BZ (2011) Aggregation-induced emission. Chem Soc Rev 40:5361CrossRef

25.

Kamikawa Y, Kato T (2007) Color-tunable fluorescent organogels: columnar self-assembly of pyrene-containing oligo(glutamic acid)s. Langmuir 23:274CrossRef

26.

Yan N, Xu Z, Diehn KK, Raghavan SR, Fang Y, Weiss RG (2013) Pyrenyl-linker-glucono gelators. Correlations of gel properties with gelator structures and characterization of solvent effects. Langmuir 29:793CrossRef

27.

Braga D, d’Agostino S, D’Amen E, Grepioni F (2011) Polymorphs from supramolecular gels: four crystal forms of the same silver(i) supergelator crystallized directly from its gels. Chem Commun 47:5154CrossRef

28.

Ruiz-Palomero C, Kennedy SR, Soriano ML, Jones CD, Valcarcel M, Steed JW (2016) Pharmaceutical crystallization with nanocellulose organogels. Chem Commun 52:7782CrossRef

29.

Cayuela A, Kennedy SR, Soriano ML, Jones CD, Valcárcel M, Steed JW (2015) Fluorescent carbon dot–molecular salt hydrogels. Chem Sci 6:6139CrossRef

30.

Foster JA, PiepenbrockMarc-Oliver M, Lloyd GO, Clarke N, HowardJudith AK, Steed JW (2010) Anion-switchable supramolecular gels for controlling pharmaceutical crystal growth. Nat Chem 2:1037CrossRef

31.

Diaz Diaz D, Kuhbeck D, Koopmans RJ (2011) Stimuli-responsive gels as reaction vessels and reusable catalysts. Chem Soc Rev 40:427CrossRef

32.

Escuder B, Rodriguez-Llansola F, Miravet JF (2010) Supramolecular gels as active media for organic reactions and catalysis. New J Chem 34:1044CrossRef

33.

Rodríguez-Llansola F, Escuder B, Miravet JF (2009) Remarkable increase in basicity associated with supramolecular gelation. Org Biomol Chem 7:3091CrossRef

34.

Quesada-Perez M, Ramos J, Forcada J, Martin-Molina A (2012) Computer simulations of thermo-sensitive microgels: quantitative comparison with experimental swelling data. J Chem Phys 136:244903CrossRef

35.

Xing B, Yu C-W, Chow K-H, Ho P-L, Fu D, Xu B (2002) Hydrophobic interaction and hydrogen bonding cooperatively confer a vancomycin hydrogel: a potential candidate for biomaterials. J Am Chem Soc 124:14846CrossRef

36.

Zhou SL, Matsumoto S, Tian HD, Yamane H, Ojida A, Kiyonaka S, Hamachi I (2005) pH-Responsive shrinkage/swelling of a supramolecular hydrogel composed of two small amphiphilic molecules. Chemistry 11:1130CrossRef

37.

Shi C, Huang Z, Kilic S, Xu J, Enick RM, Beckman EJ, Carr AJ, Melendez RE, Hamilton AD (1999) The gelation of CO₂: a sustainable route to the creation of microcellular materials. Science 286:1540CrossRef

38.

Zhang M, Meng L, Cao X, Jiang M, Yi T (2012) Morphological transformation between three-dimensional gel network and spherical vesicles via sonication. Soft Matter 8:4494CrossRef

39.

Bromberg L, Temchenko M, Moeser GD, Hatton TA (2004) Thermodynamics of temperature-sensitive polyether-modified poly(acrylic acid) microgels. Langmuir 20:5683CrossRef

40.

Krieg E, Shirman E, Weissman H, Shimoni E, Wolf SG, Pinkas I, Rybtchinski B (2009) Supramolecular gel based on a perylene diimide dye: multiple stimuli responsiveness, robustness, and photofunction. J Am Chem Soc 131:14365CrossRef

41.

Komatsu H, Matsumoto S, Tamaru S-i, Kaneko K, Ikeda M, Hamachi I (2009) Supramolecular hydrogel exhibiting four basic logic gate functions to fine-tune substance release. J Am Chem Soc 131:5580CrossRef

42.

Kiyonaka S, Sugiyasu K, Shinkai S, Hamachi I (2002) First thermally responsive supramolecular polymer based on glycosylated amino acid. J Am Chem Soc 124:10954CrossRef

43.

de Loos M, Feringa BL, van Esch JH (2005) Design and application of self-assembled low molecular weight hydrogels. Eur J Org Chem 2005:3615CrossRef

44.

Tiller JC (2003) Increasing the local concentration of drugs by hydrogel formation. Angew Chem Int Ed 42:3072CrossRef

45.

Vintiloiu A, Leroux JC (2008) Organogels and their use in drug delivery–a review. J Control Release 125:179CrossRef

46.

Yagai S, Karatsu T, Kitamura A (2005) Photocontrollable self-assembly. Chemistry 11:4054CrossRef

47.

Pieroni O, Fissi A, Angelini N, Lenci F (2001) Photoresponsive polypeptides. Acc Chem Res 34:9CrossRef

48.

Tian H, Wang S (2007) Photochromic bisthienylethene as multi-function switches. Chem Commun 781

49.

Yagai S, Kitamura A (2008) Recent advances in photoresponsive supramolecular self-assemblies. Chem Soc Rev 37:1520CrossRef

50.

Xie F, Qin L, Liu M (2016) A dual thermal and photo-switchable shrinking-swelling supramolecular peptide dendron gel. Chem Commun 52:930CrossRef

51.

Yagai S, Nakajima T, Kishikawa K, Kohmoto S, Karatsu T, Kitamura A (2005) Hierarchical organization of photoresponsive hydrogen-bonded rosettes. J Am Chem Soc 127:11134CrossRef

52.

Tamai N, Miyasaka H (2000) Ultrafast dynamics of photochromic systems. Chem Rev 100:1875–1890 CrossRef

53.

Das S, Varghese S, Kumar NS (2010) Butadiene-based photoresponsive soft materials. Langmuir 26:1598CrossRef

54.

Melanie RM, Hecht S (2010) Photoswitches: from molecules to materials. Adv Mater 22:3348CrossRef

55.

Bleger D, Yu Z, Hecht S (2011) Toward optomechanics: maximizing the photodeformation of individual molecules. Chem Commun 47:12260CrossRef

56.

Murata K, Aoki M, Suzuki T, Harada T, Kawabata H, Komori T, Ohseto F, Ueda K, Shinkai S (1994) Thermal and light control of the sol-gel phase transition in cholesterol-based organic gels. Novel helical aggregation modes as detected by circular dichroism and electron microscopic observation. J Am Chem Soc 116:6664CrossRef

57.

Murata K, Aoki M, Shinkai S (1992) Sol-gel phase transition of switch-functionalized cholesterols as detected by circular dichroism. Chem Lett 21:739CrossRef

58.

Duan P, Li Y, Li L, Deng J, Liu M (2011) Multiresponsive chiroptical switch of an azobenzene-containing lipid: solvent, temperature, and photoregulated supramolecular chirality. J Phys Chem B 115:3322CrossRef

59.

Wu Y, Wu S, Tian X, Wang X, Wu W, Zou G, Zhang Q (2011) Photoinduced reversible gel–sol transitions of dicholesterol-linked azobenzene derivatives through breaking and reforming of van der Waals interactions. Soft Matter 7:716CrossRef

60.

Ran X, Wang H, Zhang P, Bai B, Zhao C, Yu Z, Li M (2011) Photo-induced fiber–vesicle morphological change in an organogel based on an azophenyl hydrazide derivative. Soft Matter 7:8561CrossRef

61.

Koehler JM, Mueller SC (1995) Frozen chemical waves in the belousov-zhabotinsky reaction. J Phys Chem 99:980CrossRef

62.

Li Y, Tanaka Toyoichi (1990) Kinetics of swelling and shrinking of gels. J Chem Phys 92:1365CrossRef

63.

Xu JF, Chen YZ, Wu D, Wu LZ, Tung CH, Yang QZ (2013) Photoresponsive hydrogen-bonded supramolecular polymers based on a stiff stilbene unit. Angew Chem Int Ed 52:9738CrossRef

64.

Draper ER, Eden EG, McDonald TO, Adams DJ (2015) Spatially resolved multicomponent gels. Nat Chem 7:848CrossRef

65.

Zhu L, Li X, Zhang Q, Ma X, Li M, Zhang H, Luo Z, Agren H, Zhao Y (2013) Unimolecular photoconversion of multicolor luminescence on hierarchical self-assemblies. J Am Chem Soc 135:5175CrossRef

66.

Srivastava A, Ghorai S, Bhattacharjya A, Bhattacharya S (2005) A tetrameric sugar-based azobenzene that gels water at various pH values and in the presence of salts. J Org Chem 70:6574CrossRef

67.

Yagai S, Karatsu T, Kitamura A (2005) Melamine-barbiturate/cyanurate binary organogels possessing rigid azobenzene-tether moiety. Langmuir 21:11048CrossRef

68.

Miljanić S, Frkanec L, Meić Z, Žinić M (2005) Photoinduced gelation by stilbene oxalyl amide compounds. Langmuir 21:2754CrossRef

69.

Yagai S, Ishiwatari K, Lin X, Karatsu T, Kitamura A, Uemura S (2013) Rational design of photoresponsive supramolecular assemblies based on diarylethene. Chem Eur J 19:6971CrossRef

70.

Yarimaga O, Jaworski J, Yoon B, Kim JM (2012) Polydiacetylenes: supramolecular smart materials with a structural hierarchy for sensing, imaging and display applications. Chem Commun 48:2469CrossRef

71.

Neabo JR, Rondeau-Gagne S, Vigier-Carriere C, Morin JF (2013) Soluble conjugated one-dimensional nanowires prepared by topochemical polymerization of a butadiynes-containing star-shaped molecule in the xerogel state. Langmuir 29:3446CrossRef

72.

Aoki K, Kudo M, Tamaoki N (2004) Novel odd/even effect of alkylene chain length on the photopolymerizability of organogelators. Org Lett 6:4009CrossRef

73.

Fujita N, Sakamoto Y, Shirakawa M, Ojima M, Fujii A, Ozaki M, Shinkai S (2007) Polydiacetylene nanofibers created in low-molecular-weight gels by post modification: control of blue and red phases by the odd−even effect in alkyl chains. J Am Chem Soc 129:4134CrossRef

74.

Minkin VI (2004) Photo-, thermo-, solvato-, and electrochromic spiroheterocyclic compounds. Chem Rev 104:2751CrossRef

75.

Berkovic G, Nuclear S, Krongauz V (2000) Spiropyrans and spirooxazines for memories and switches. Chem Rev 100:1741CrossRef

76.

Raymo FM, Tomasulo M (2005) Electron and energy transfer modulation with photochromic switches. Chem Soc Rev 34:327CrossRef

77.

Qiu Z, Yu H, Li J, Wang Y, Zhang Y (2009) Spiropyran-linked dipeptide forms supramolecular hydrogel with dual responses to light and to ligand-receptor interaction. Chem Commun 0:3342

78.

Li Y, Wong KM, Tam AY, Wu L, Yam VW (2010) Thermo- and acid-responsive photochromic spironaphthoxazine-containing organogelators. Chem Eur J 16:8690CrossRef

79.

Chen Q, Feng Y, Zhang D, Zhang G, Fan Q, Sun S, Zhu D (2010) Light-triggered self-assembly of a spiropyran-functionalized dendron into nano-/micrometer-sized particles and photoresponsive organogel with switchable fluorescence. Adv Funct Mater 20:36CrossRef

80.

Irie M (2000) Diarylethenes for memories and switches. Chem Rev 100:1685CrossRef

81.

Praveen VK, George SJ, Varghese R, Vijayakumar C, Ajayaghosh A (2012) A smart gelator as a chemosensor: application to integrated logic gates in solution, gel, and film. Chem Eur J 18:3549CrossRef

82.

Foster JA, Parker RM, Belenguer AM, Kishi N, Sutton S, Abell C, Nitschke JR (2015) Differentially addressable cavities within metal-organic cage-cross-linked polymeric hydrogels. J Am Chem Soc 137:9722CrossRef

83.

de Jong JJD, Lucas LN, Kellogg RM, van Esch JH, Feringa BL (2004) Reversible optical transcription of supramolecular chirality into molecular chirality. Science 304:278CrossRef

84.

Xiao S, Zou Y, Yu M, Yi T, Zhou Y, Li F, Huang C (2007) A photochromic fluorescent switch in an organogel system with non-destructive readout ability. Chem Commun 4758

85.

de Jong JJ, Browne WR, Walko M, Lucas LN, Barrett LJ, McGarvey JJ, van Esch JH, Feringa BL (2006) Raman scattering and FT-IR spectroscopic studies on dithienylethene switches-towards non-destructive optical readout. Org Biomol Chem 4:2387CrossRef

86.

Tian H, Yang S (2004) Recent progresses on diarylethene based photochromic switches. Chem Soc Rev 33:85CrossRef

87.

Andréasson J, Pischel U (2010) Smart molecules at work-mimicking advanced logic operations. Chem Soc Rev 39:174

88.

Andreasson J, Pischel U, Straight SD, Moore TA, Moore AL, Gust D (2011) All-photonic multifunctional molecular logic device. J Am Chem Soc 133:11641CrossRef

89.

Cravotto G, Cintas P (2009) Molecular self-assembly and patterning induced by sound waves. The case of gelation. Chem Soc Rev 38:2684CrossRef

90.

Paulusse JM, Sijbesma RP (2006) Molecule-based rheology switching. Angew Chem Int Ed 45:2334CrossRef

91.

Gerber TP, Hout M (1998) More shock than therapy: market transition, employment, and income in Russia, 1991–1995. Am J Sociol 104:1CrossRef

92.

Sijbesma RP, Beijer FH, Brunsveld L, Folmer BJB, Hirschberg JHKK, Lange RFM, Lowe JKL, Meijer EW (1997) Reversible polymers formed from self-complementary monomers using quadruple hydrogen bonding. Science 278:1601CrossRef

93.

Wu J, Yi T, Xia Q, Zou Y, Liu F, Dong J, Shu T, Li F, Huang C (2009) Tunable gel formation by both sonication and thermal processing in a cholesterol-based self-assembly system. Chem Eur J 15:6234CrossRef

94.

Jadhav SR, Vemula PK, Kumar R, Raghavan SR, John G (2010) Sugar-derived phase-selective molecular gelators as model solidifiers for oil spills. Angew Chem Int Ed 49:7695CrossRef

95.

Mukherjee S, Mukhopadhyay B (2012) Phase selective carbohydrate gelator. RSC Adv 2:2270CrossRef

96.

Blanco E, Esquivias L, Litrán R, Piñero M, Ramírez-del-Solar M, de la Rosa-Fox N (1999) Sonogels and derived materials. Appl Organometal Chem 13:399CrossRef

97.

Bardelang D (2009) Ultrasound induced gelation: a paradigm shift. Soft Matter 5:1969CrossRef

98.

Cai X, Wu Y, Wang L, Yan N, Liu J, Fang X, Fang Y (2013) Mechano-responsive calix[4]arene-based molecular gels: agitation induced gelation and hardening. Soft Matter 9:5807CrossRef

99.

Anderson KM, Day GM, Paterson MJ, Byrne P, Clarke N, Steed JW (2008) Structure calculation of an elastic hydrogel from sonication of rigid small molecule components. Angew Chem Int Ed 47:1058CrossRef

100.

Yu X, Cao X, Chen L, Lan H, Liu B, Yi T (2012) Thixotropic and self-healing triggered reversible rheology switching in a peptide-based organogel with a cross-linked nano-ring pattern. Soft Matter 8:3329CrossRef

101.

Wang R-Y, Liu X-Y, Li J-L (2009) Engineering molecular self-assembled fibrillar networks by ultrasound. Cryst Growth Des 9:3286CrossRef

102.

Cao Y, Tang LM, Wang YJ, Zhang BY, Jia LK (2008) Influence of ultrasound treatment on assembling structures and properties of supramolecular hydrogels formed from 1,3,5-benzenetricarboxylic acid and 4-hydroxypyridine. Chem Lett 37:554CrossRef

103.

van Herpt JT, Stuart MC, Browne WR, Feringa BL (2013) Mechanically induced gel formation. Langmuir 29:8763CrossRef

104.

Yu X, Liu Q, Wu J, Zhang M, Cao X, Zhang S, Wang Q, Chen L, Yi T (2010) Sonication-triggered instantaneous gel-to-gel transformation. Chem Eur J 16:9099CrossRef

105.

Naota T, Koori H (2005) Molecules that assemble by sound: an application to the instant gelation of stable organic fluids. J Am Chem Soc 127:9324CrossRef

106.

Yaobing Wang CZ, Fu H, Li X, Sheng X, Zhao Y, Xiao D, Ma Y, Ma JS, Yao Jiannian (2008) Switch from intra- to intermolecular H-bonds by ultrasound: induced gelation and distinct nanoscale morphologies. Langmuir 24:7635CrossRef

107.

Liu K, Meng L, Mo S, Zhang M, Mao Y, Cao X, Huang C, Yi T (2013) Colour change and luminescence enhancement in a cholesterol-based terpyridyl platinum metallogel via sonication. J Mater Chem C 1:1753CrossRef

108.

Chen Q, Zhang D, Zhang G, Yang X, Feng Y, Fan Q, Zhu D (2010) Multicolor tunable emission from organogels containing tetraphenylethene, perylenediimide, and spiropyran derivatives. Adv Funct Mater 20:3244CrossRef

109.

Mahesh S, Thirumalai R, Yagai S, Kitamura A, Ajayaghosh A (2009) Role of complementary H-bonding interaction of a cyanurate in the self-assembly and gelation of melamine linked tri(p-phenyleneethynylene)s. Chem Commun 5984

110.

Li JL, Liu XY (2010) Architecture of supramolecular soft functional materials: from understanding to micro-/nanoscale engineering. Adv Funct Mater 20:3196CrossRef

111.

Bardelang D, Zaman MB, Moudrakovski IL, Pawsey S, Margeson JC, Wang D, Wu X, Ripmeester JA, Ratcliffe CI, Yu K (2008) Interfacing supramolecular gels and quantum dots with ultrasound: smart photoluminescent dipeptide gels. Adv Mater 20:4517CrossRef

112.

Gaponik N, Wolf A, Marx R, Lesnyak V, Schilling K, Eychmüller A (2008) Three-dimensional self-assembly of thiol-capped CdTe nanocrystals: gels and aerogels as building blocks for nanotechnology. Adv Mater 20:4257CrossRef

113.

Wu J, Tian Q, Hu H, Xia Q, Zou Y, Li F, Yi T, Huang C (2009) Self-assembly of peptide-based multi-colour gels triggered by up-conversion rare earth nanoparticles. Chem Commun 4100

114.

Brochu AB, Craig SL, Reichert WM (2011) Self-healing biomaterials. J Biomed Mater Res A 96:492CrossRef

115.

Hager MD, Greil P, Leyens C, van der Zwaag S, Schubert US (2010) Self-healing materials. Adv Mater 22:5424CrossRef

116.

Huang X, Raghavan SR, Terech P, Weiss RG (2006) Distinct kinetic pathways generate organogel networks with contrasting fractality and thixotropic properties. J Am Chem Soc 128:15341CrossRef

117.

Vemula PK, John G (2008) Crops: a green approach toward self-assembled soft materials. Acc Chem Res 41:769CrossRef

118.

Bhattacharya S, Krishnan Ghosh Y (2001) First report of phase selective gelation of oil from oil/water mixtures. Possible implications toward containing oil spills. Chem Commun 185

119.

Abe S, Endo M, Sato M, Awano K (1996) Solid-liquid extraction of metal ions with thixotropic gels. Anal Commun 33:137CrossRef

120.

Yan J, Liu J, Lei H, Kang Y, Zhao C, Fang Y (2015) Ferrocene-containing thixotropic molecular gels: creation and a novel strategy for water purification. J Colloid Interface Sci 448:374CrossRef

121.

Carretti E, Bonini M, Dei L, Berrie BH, Angelova LV, Baglioni P, Weiss RG (2010) New frontiers in materials science for art conservation: responsive gels and beyond. Acc Chem Res 43:751CrossRef

122.

Sun K, Oh H, Emerson JF, Raghavan SR (2012) A new method for centrifugal separation of blood components: creating a rigid barrier between density-stratified layers using a UV-curable thixotropic gel. J Mater Chem 22:2378CrossRef

123.

Rodriguez-Llansola F, Escuder B, Miravet JF, Hermida-Merino D, Hamley IW, Cardin CJ, Hayes W (2010) Selective and highly efficient dye scavenging by a pH-responsive molecular hydrogelator. Chem Commun 46:7960CrossRef

124.

Miravet JF, Escuder B (2005) Pyridine-functionalised ambidextrous gelators: towards catalytic gels. Chem Commun 5796

125.

Adams DJ, Butler MF, Frith WJ, Kirkland M, Mullen L, Sanderson P (2009) A new method for maintaining homogeneity during liquid–hydrogel transitions using low molecular weight hydrogelators. Soft Matter 5:1856CrossRef

126.

Samanta K, Ehlers M, Schmuck C (2016) Two-component self-assembly: hierarchical formation of pH-switchable supramolecular networks by π-π induced aggregation of ion pairs. Chem Eur J 22:15242CrossRef

127.

Tena-Solsona M, Alonso-de Castro S, Miravet JF, Escuder B (2014) Co-assembly of tetrapeptides into complex pH-responsive molecular hydrogel networks. J Mater Chem B 2:6192CrossRef

128.

Jeppesen JO, Nielsen MB, Becher J (2004) Tetrathiafulvalene cyclophanes and cage molecules. Chem Rev 104:5115CrossRef

129.

Canevet D, Salle M, Zhang G, Zhang D, Zhu D (2009) Tetrathiafulvalene (TTF) derivatives: key building-blocks for switchable processes. Chem Commun 2245

130.

Wang C, Zhang D, Zhu D (2005) A low-molecular-mass gelator with an electroactive tetrathiafulvalene group: tuning the gel formation by charge-transfer interaction and oxidation. J Am Chem Soc 127:16372CrossRef

131.

Wang C, Chen Q, Sun F, Zhang D, Zhang G, Huang Y, Zhao R, Zhu D (2010) Multistimuli responsive organogels based on a new gelator featuring tetrathiafulvalene and azobenzene groups: reversible tuning of the gel−sol transition by redox reactions and light irradiation. J Am Chem Soc 132:3092CrossRef

132.

Liu J, He P, Yan J, Fang X, Peng J, Liu K, Fang Y (2008) An organometallic super-gelator with multiple-stimulus responsive properties. Adv Mater 20:2508CrossRef

133.

Kawano S, Fujita N, Shinkai S (2005) Quater-, quinque-, and sexithiophene organogelators: unique thermochromism and heating-free sol-gel phase transition. Chem Eur J 11:4735CrossRef

134.

Ikeda M, Tanida T, Yoshii T, Hamachi I (2011) Rational molecular design of stimulus-responsive supramolecular hydrogels based on dipeptides. Adv Mater 23:2819CrossRef

135.

Steed JW (2010) Anion-tuned supramolecular gels: a natural evolution from urea supramolecular chemistry. Chem Soc Rev 39:3686CrossRef

136.

Yamanaka M, Nakamura T, Nakagawa T, Itagaki H (2007) Reversible sol–gel transition of a tris–urea gelator that responds to chemical stimuli. Tetrahedron Lett 48:8990CrossRef

137.

Džolić Z, Cametti M, Dalla Cort A, Mandolini L,Žinić M (2007) Fluoride-responsive organogelator based on oxalamide-derived anthraquinone. Chem Commun 3535

138.

Kim H-J, Zin W-C, Lee M (2004) Anion-directed self-assembly of coordination polymer into tunable secondary structure. J Am Chem Soc 126:7009CrossRef

139.

Sobczuk AA, Tamarua S, Shinkai S (2011) New strategy for controlling the oligothiophene aggregation mode utilizing the gel-to-sol phase transition induced by crown-alkali metal interactions. Chem Commun 47:3093CrossRef

140.

Brignell SV, Smith DK (2007) Crown ether functionalised dendrons—controlled binding and release of dopamine in both solution and gel-phases. New J Chem 31:1243CrossRef

141.

Edwards W, Smith DK (2012) Cation-responsive silver-selective organogel-exploiting silver-alkene interactions in the gel-phase. Chem Commun 48:2767CrossRef

142.

Jin Q, Zhang L, Zhu X, Duan P, Liu M (2012) Amphiphilic Schiff base organogels: metal-ion-mediated chiral twists and chiral recognition. Chem Eur J 18:4916CrossRef

143.

Mukhopadhyay P, Iwashita Y, Shirakawa M, Kawano S, Fujita N, Shinkai S (2006) Spontaneous colorimetric sensing of the positional isomers of dihydroxynaphthalene in a 1D organogel matrix. Angew Chem Int Ed 45:1592CrossRef

144.

Tazawa T, Yagai S, Kikkawa Y, Karatsu T, Kitamura A, Ajayaghosh A (2010) A complementary guest induced morphology transition in a two-component multiple H-bonding self-assembly. Chem Commun 46:1076CrossRef

145.

Deng W, Yamaguchi H, Takashima Y, Harada A (2007) A chemical-responsive supramolecular hydrogel from modified cyclodextrins. Angew Chem Int Ed 46:5144CrossRef

146.

Chen X, Huang Z, Chen SY, Li K, Yu X-Q, Pu L (2010) Enantioselective gel collapsing: a new means of visual chiral sensing. J Am Chem Soc 132:7297CrossRef

147.

Tu T, Fang W, Bao X, Li X, Dotz KH (2011) Visual chiral recognition through enantioselective metallogel collapsing: synthesis, characterization, and application of platinum-steroid low-molecular-mass gelators. Angew Chem Int Ed 50:6601CrossRef

Titel: Supramolecular Gels
verfasst von: Jianyong Zhang
Ya Hu
Yongguang Li
Verlag: Springer Singapore
Buch: Gel Chemistry
Print ISBN: 978-981-10-6880-5

Electronic ISBN: 978-981-10-6881-2

Copyright-Jahr: 2018
DOI: https://doi.org/10.1007/978-981-10-6881-2_2

Premium Partner

Marktübersichten

Die im Laufe eines Jahres in der „adhäsion“ veröffentlichten Marktübersichten helfen Anwendern verschiedenster Branchen, sich einen gezielten Überblick über Lieferantenangebote zu verschaffen.

Zur Marktübersicht