Polymers molecular recognition

L. Pu, l,l -Binaphthyl Dimers, Oligomers and Polymers Molecular Recognition, Asymmetric Catalysis and New Materials, Chem. Rev. 1998, 98, 2405-2494. 

Keywords Adaptive chemistry Dynamic networks Dynamic polymers Molecular recognition Multiple dynamics Self-organization Supramolecular chemistry... 

Takeuchi T, Mukawa T, Shinmori H (2005) Signaling molecularly imprinted polymers Molecular recognition-based sensing materials. Chem Rec 5 263... 

Billingham, N. C., and Calvert, R D., Electrically conducting polymers—a polymer science viewpoint, in Conducting Polymers/Molecular Recognition, Advances in Polymer Science, Vol. 90, Springer-Verlag, Berlin, 1989, pp. 1-104. 

Conducting Polymers - Molecular Recognition, Advances in Polymer Science Series No. 90, Springer-Verlag, New York (1989). 

However, all the receptors hitherto discussed are monomolecular species which possess a monomolecular cavity, pocket, cleft, groove or combination of it including the recognition sites to yield a molecular receptor—substrate complex. They can be assembled and preserved ia solution although there are dependences (see below). By way of contrast, molecular recognition demonstrated ia the foUowiag comes from multimolecular assembly and organization of a nonsolution phase such as polymer materials and crystals. 

Much attention has recently been focused on organoboronic acids and their esters because of their practical usefulness for synthetic organic reactions including asymmetric synthesis, combinatorial synthesis, and polymer synthesis [1, 3, 7-9], molecular recognition such as host-guest compounds [10], and neutron capture therapy in treatment of malignant melanoma and brain tumor ]11]. New synthetic procedures reviewed in this article wiU serve to find further appHcations of organoboron compounds. 

COlfen H (2007) Bio-inspired Mineralization Using Hydrophilic Polymers. 271 1-77 Collin J-P, Heitz V, Sauvage J-P (2005) Transition-Metal-Complexed Catenanes and Rotax-anes in Motion Towards Molecular Machines. 262 29-62 Collins BE, Wright AT, Anslyn EV (2007) Combining Molecular Recognition, Optical Detection, and Chemometric Analysis. 277 181-218 Collyer SD, see Davis F (2005) 255 97-124 Commeyras A, see Pascal R (2005) 259 69-122 Coquerel G (2007) Preferential Crystallization. 269 1-51 Correia JDG, see Santos I (2005) 252 45-84 Costanzo G, see Saladino R (2005) 259 29-68 Cotarca L, see Zonta C (2007) 275 131-161 Credi A, see Balzani V (2005) 262 1-27 Crestini C, see Saladino R (2005) 259 29-68... 

Crystalline fructose, 23 485-486 Crystalline glycolic acid, 14 127 Crystalline hybrid compounds, 13 546-548 Crystalline inclusion compounds, 14 184 molecular recognition behavior of, 16 796 preparation of, 14 182 Crystalline melting point, of polymers, 20 399... 

To prepare artificial enzymatic systems possessing molecular recognition ability for particular molecules, molecular imprinting methods that create template-shaped cavities with the memory of the template molecules in polymer matrices, have been developed [22, 30-35] and established in receptor, chromatographical separations, fine-chemical sensing, etc. in the past decade. The molecular... 

Fan L-J, Zhanga Y, Murphy CB, Angell SE, Parker MFL, Flynn BR, Jones WE Jr (2009) Fluorescent conjugated polymer molecular wire chemosensors for transition metal ion recognition and signaling. Coord Chem Rev 253 401 122... 

Molecular imprinting has recently attracted considerable attention as an approach to the preparation of polymers containing recognition sites with predetermined selectivity. The history and specifics of the imprinting technique pioneered by Wulff in the 1970s have been detailed in several excellent review articles [122-124]. Imprinted monoliths have also received attention as stationary phases for capillary electrochromatography. 

Different classifications for the chiral CSPs have been described. They are based on the chemical structure of the chiral selectors and on the chiral recognition mechanism involved. In this chapter we will use a classification based mainly on the chemical structure of the selectors. The selectors are classified in three groups (i) CSPs with low-molecular-weight selectors, such as Pirkle type CSPs, ionic and ligand exchange CSPs, (ii) CSPs with macrocyclic selectors, such as CDs, crown-ethers and macrocyclic antibiotics, and (iii) CSPs with macromolecular selectors, such as polysaccharides, synthetic polymers, molecular imprinted polymers and proteins. These different types of CSPs, frequently used for the analysis of chiral pharmaceuticals, are discussed in more detail later. 

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Fouquey, C. Lehn, J.-M. Levelut, A.-M. Molecular recognition directed self-assembly of supramolecular liquid crystalline polymers from complementary chiral components. Adv. Mater. 1990, 2, 254-257. 

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