Recognition, polymer

Yoshida, M. Hatate, Y. Uezu, K. Goto, M. Furusaki, S., Chiral-recognition polymer prepared by surface molecular imprinting technique, Colloids Surf A. 2000, 169, 259-269... 

Bian Q, Xiao Y, Lang M (2012) ThomOTesponsive biotinylated star amphiphilic block copolymer synthesis, self-assembly, and specific taiget recognition. Polymer 53 1684-1693... 

Ikegami, T. Mukawa, T. Nariai, H. Takeuchi, T. (2004). Bisphenol A-recognition polymers prepared by covalent molecular imprinting. Analytica Chimica Acta, 504, 131-135. 

Many complex systems have been spread on liquid interfaces for a variety of reasons. We begin this chapter with a discussion of the behavior of synthetic polymers at the liquid-air interface. Most of these systems are linear macromolecules however, rigid-rod polymers and more complex structures are of interest for potential optoelectronic applications. Biological macromolecules are spread at the liquid-vapor interface to fabricate sensors and other biomedical devices. In addition, the study of proteins at the air-water interface yields important information on enzymatic recognition, and membrane protein behavior. We touch on other biological systems, namely, phospholipids and cholesterol monolayers. These systems are so widely and routinely studied these days that they were also mentioned in some detail in Chapter IV. The closely related matter of bilayers and vesicles is also briefly addressed. 

Recognition of these differences in behavior points out an important limitation on the copolymer composition equation. The equation describes the overall composition of the copolymer, but gives no information whatsoever about the distribution of the different kinds of repeat units within the polymer. While the overall composition is an important property of the copolymer, the details of the microstructural arrangement is also a significant feature of the molecule. It is possible that copolymers with the same overall composition have very different properties because of differences in microstructure. Reviewing the three categories presented in Chap. 1, we see the following ... 

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. 

MgCl2-Supported Catalysts. Examination of polymerizations with TiCl catalysts has estabUshed that only a small percentage of titanium located on lateral faces, edges, and along crystal defects is active (52) (see Titanium and titanium alloys). This led to the recognition that much of the catalyst mass acted only as a support, promoting considerable activity aimed at finding a support for active titanium that would not be detrimental to polymer properties. 

The main benefit of the Dow process was control of the polymer architecture. The polymer from the self-condensation process possessed a linear stmcture, but there were other difficulties. The monomer was cosdy and removal of the cuprous bromide by-product was difficult (17) ultimately, scale-up difficulties terrninated the Dow PPS development. However, there was a growing recognition that PPS was an attractive polymer with an excellent combination of properties. 

The development of highly selective chemical sensors for complex matrixes of medical, environmental, and industrial interest has been the object of greate research efforts in the last years. Recently, the use of artificial materials - molecularly imprinted polymers (MIPs) - with high recognition properties has been proposed for designing biomimetic sensors, but only a few sensor applications of MIPs based on electrosynythesized conductive polymers (MIEPs) have been reported [1-3]. 

P. B. Harrington, K. J. Voorhees, T. E. Street, F. Radicati di Brozolo, and R. W. Odom. Anal Chem. 61, 715, 1989. Presents a discussion of LIMS polymer analysis and pattern recognition techniques. 

This episode has been displayed in some detail because colloid science is a clear instance of a major field of research which has never quite succeeded in gaining recognition as a distinct discipline, in spite of determined attempts by a number of its practitioners. The one feature that most distinguishes colloid science from physical chemistry, polymer science and chemical engineering is that universities have not awarded degrees in colloid science. That is, perhaps, what counts most for fields with ambitions to become fullblown disciplines. 

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