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Towards a universal organogelator:A general mixing approach to fabricate various organic compounds into organogels 被引量:5

Towards a universal organogelator:A general mixing approach to fabricate various organic compounds into organogels
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摘要 Low-molecular-weight organogels(LMOG) have been attracting a surge interest in fabricating soft materials.Although the finding of the gelator molecules has been developed from serendipity to objective design,the achievement of the gelator molecules still needs good design and tedious organic synthesis.In this paper,we proposed a simple and general mixing approach to get the organogel for nearly all the organic compounds and even soluble nanoparticles without any modification.We have designed a universal gelator molecule,which forms organogels with more than 40 kinds of organic solvents from aploar to polar solvents.More interestingly,when other organic compounds or even nanomaterials,which are soluble in certain organic solvents,are mixed with this gelator molecule,they can form organogels no matter whether the individual compounds could form organogel or not.This method is applicable to nearly all kinds of soluble organic compounds and opens an efficient and universal way to fabricate gel materials. Low-molecular-weight organogels (LMOG) have been attracting a surge interest in fabricating soft materials. Although the finding of the gelator molecules has been developed from serendipity to objective design, the achievement of the gelator molecules still needs good design and tedious organic synthesis. In this paper, we proposed a simple and general mixing approach to get the organogel for nearly all the organic compounds and even soluble nanoparticles without any modification. We have designed a universal gelator molecule, which forms organogels with more than 40 kinds of organic solvents from aploar to polar solvents. More interestingly, when other organic compounds or even nanomaterials, which are soluble in certain organic solvents, are mixed with this gelator molecule, they can form organogels no matter whether the individual compounds could form organogel or not. This method is applicable to nearly all kinds of soluble organic compounds and opens an efficient and universal way to fabricate gel materials.
出处 《Science China Chemistry》 SCIE EI CAS 2011年第7期1051-1063,共13页 中国科学(化学英文版)
基金 supported by the National Natural Science Foundation of China (50673095 and 21021003) the Basic Research Development Program (2007CB808005 and 2009CB930802) the Fund of the Chinese Academy of Sciences
关键词 有机化合物 混合 低分子量 制作 有机凝胶 有机溶剂 软质材料 有机合成 organogel, hybrid system, supramolecular chemistry, self-assembly, soft matter
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参考文献67

  • 1DUAN PengFei,LI YuanGang,LIU MingHua.Preparation of optical active polydiacetylene through gelating and the control of supramolecular chirality[J].Science China Chemistry,2010,53(2):432-437. 被引量:4
  • 2Mohan SRK,Hamachi I.Synthesis of new supramolecular polymers based on glycosylated amino acid and their applications. Current Organic Chemistry . 2005
  • 3Ajayaghosh A,Praveen VK.pi-organogels of self-assembled p-phenylenevinylenes: Soft materials with distinct size,shape,and functions. Accounts of Chemical Research . 2007
  • 4Hirst AR,Coates IA,Boucheteau TR,Miravet JF,Escuder B,Castelletto V,Hamley IW,Smith DK.Low-molecular-weight gelators: Elucidating the principles of gelation based on gelator solubility and a cooperative self-assembly model. Journal of the American Chemical Society . 2008
  • 5Dawn A,Fujita N,Haraguchi S,Sada K,Shinkai S.An organogel system can control the stereochemical course of anthracene photodimerization. Chemical Communications . 2009
  • 6Page MG,Warr GG.Influence of the structure and composition of mono- and dialkyl phosphate mixtures on aluminum complex organogels. Langmuir . 2009
  • 7George M,,Snyder SL,Terech P,Glinka CJ,Weiss RG.N-alkyl perfluoroalkanamides as low molecular-mass organogelators. Journal of the American Chemical Society . 2003
  • 8Kida T,Marui Y,Miyawaki K,Kato E,Akashi M.Unique organogel formation with a channel-type cyclodextrin assembly. Chemical Communications . 2009
  • 9Yagai S,Nakajima T,Kishikawa K,Kohmoto S,Karatsu T,Kitamura A.Hierarchical organization of photoresponsive hydrogen- bonded rosettes. Journal of the American Chemical Society . 2005
  • 10Wang C,Zhang DQ,Xiang JF,Zhu DB.New organogels based on an anthracene derivative with one urea group and its photodimer: Fluorescence enhancement after gelation. Langmuir . 2007

二级参考文献31

  • 1Fujiki M,,Koe JR,Terao K,Sato T,Teramoto A,Watanabe J.Opti- cally active polysilanes. Ten years of progress and new polymer twist for nanoscience and nanotechnology. Polymer Journal . 2003
  • 2Reppy MA,Pindzola BA.Biosensing with polydiacetylene materials: structures, optical properties and applications. Chemical Communications . 2007
  • 3Masuda M,Hanada T,Okada Y,Yase K,Shimizu T.Polymerization in nanometer-sized fibers: Molecular packing order and polymeriza- bility. Macromolecules . 2000
  • 4Deb P,Yuan ZZ,Ramsey L,Hanks TW.Synthesis and optical prop- erties of chiral polydiacetylenes. Macromolecules . 2007
  • 5Hsu L,Cvetanovich GL,Stupp SI.Peptide amphiphile nanofibers with conjugated polydiacetylene backbones in their core. Journal of the American Chemical Society . 2008
  • 6Wilson RB.Diacetylene monomers and polymers with chiral sub- stituents: Structure, solid-state polymerization, and properties. Journal of the American Chemical Society . 1982
  • 7Wenz G,Mueller MA,Schmidt M,Wegner G.Structure of poly(diacetylenes) in solution. Macromolecules . 1984
  • 8Hoebin F J M,Jonkheijm P,Meijer E W,et al.About supramolecular self-assemblies of π-conjugated systems. Chemical Reviews . 2005
  • 9E. Yashima,,K. Maeda,Y. Okamoto.Memory of macromolecular helicity assisted by interaction with achiral small molecules. Nature . 1999
  • 10Hopkins,T.E.,Wagener,K.B.Chiral polyolefins. Advanced Materials . 2002

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同被引文献34

  • 1DUAN PengFei,LI YuanGang,LIU MingHua.Preparation of optical active polydiacetylene through gelating and the control of supramolecular chirality[J].Science China Chemistry,2010,53(2):432-437. 被引量:4
  • 2GEORGE M, WEISS R G. Molecular organogels. Soft matter com- prised of low-molecular-mass organic gelators and organic liquids [ J ]. Accounts of Chemical Research ,2006,39 ( 8 ) :489-497.
  • 3ESTROFF L A, HAMILTON A D. Water gclation by small organic molecules[ J ]. Chemical Reviews,2004,104 ( 3 ) : 1201 - 1217.
  • 4SANGEETHA N M, MAITRA U. Supramolecular gels: Functions and us[ J]. Chemical Society Reviews,2005,34(10) :821-836.
  • 5LLUSAR M ,SANCHEZ C. Inorganic and hybrid nanofibrous mate- rials templated with organogelators [ J ]. Chemistry of Materials, 2008,20( 3 ) :782-820.
  • 6DOLORES S M M,NEBOT V J, MIRAVET J F,et al. Control of molecular gelation by chemical stimuli [ J ]. Chemical Society Re- views, 2013,42 ( 17 ) : 7086 -7098.
  • 7HIRST A R,ESCUDER B,M1RAVET J F,et al. High-Tech appli- cations of self-assembling supramolecular nanostructured gel-phase materials:from regenerative medicine to electronic devices[ J ]. An- gewandte Chemic-lnternational Edition, 2008, 47 ( 42 ) : 8002 -8018.
  • 8TIAN H, WANG S. Photochromic bisthienylethene as multi-function switches[ J ]. Chemical Communications ,2007,44(8 ) :781-792.
  • 9JIN Q, ZHANG L, CAO H, et al. Self-assembly of copper( Ⅱ ) ion- mediated nanotube and its supramolecular chiral catalytic behavior [ J ]. Langmuir,2011,27 (22) : 13847-13853.
  • 10DAI L,TU T,YOU S,et al. Asymmetric catalysis with chirul ferro- cene ligands[ J ]. Accounts of Chemical Research, 2003,36 ( 9 ) : 659-667.

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