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Molecular recognition hydrogen bonding

Our discussion in this chapter will focus on the use of the electrostatic potential as a means to understanding and predicting chemical interactions. First, we will examine some of its properties and important features. Next, we will discuss methodology. Finally we will review some recent applications of the electrostatic potential in areas such as hydrogen bonding, molecular recognition, and understanding and prediction of a variety of physio-chemical properties related to molecular interactions. Our intent has not been to provide a complete survey of the ways in which the potential has been used, many of which are described elsewhere (Politzer and Daiker 1981 Politzer, Laurence, and Jayasuriya 1985 Politzer and Murray 1990 Politzer and Murray 1991 Politzer and Truhlar 1981 Scrocco and Tomasi 1973), but rather to focus on some diverse examples. [Pg.50]

Keywords Hydrogen bonding, Molecular recognition. Self-assembly, Complexation, Heterocyclic compounds... [Pg.63]

Figure 6 Assembly of bis-ureas through the formation of self-complementary hydrogen-bonding molecular recognition pathways. Figure 6 Assembly of bis-ureas through the formation of self-complementary hydrogen-bonding molecular recognition pathways.
Perrault, D. M., Chen, X., and Anslyn, E. V. "The Advantages of Using Rigid Polyaza-Clefts for Hydrogen-Bonding Molecular Recognition." Tetrahedron, 51,353-362 (1995). [Pg.257]

Gong B, Yan YF, Zeng HQ, Skrzypczak-Jankunn E, Kim YW, Zhu J, Ickes H. A new approach for the design of supramolecular recognition units hydrogen-bonded molecular duplexes. J Am Chem Soc 1999 121 5607-5608. [Pg.232]

Key words. Recognition, hydrogen bonding, molecular clefts, convergent functionality, concerted catalysis, stereoelectronic effects. [Pg.8]

This term is an explicit recognition of the importance of hydrogen bonding to molecular Iriieraciions. [Pg.179]

Fersht, A.R. The hydrogen bond in molecular recognition. Trends Biochem. Sci. 12 301-304, 1987. [Pg.371]

Molecular recognition of nucleobases and nucleotides at air-water interfaces (complementary hydrogen bonding and multisite interaction) 98ACR371. [Pg.262]

Apart from the successful imprinting discussed above, the recognition for many templates is far from that is required for the particular application, even after careful optimization of the other factors affecting the molecular recognition properties. Often, a large excess of MAA in the synthesis step is required for recognition to be observed and then only in solvents of low to medium polarity and hydrogen bond... [Pg.168]

Paldus J, Li X (1999) Electron Correlation in Small Molecules Grafting Cl onto CC. 203 1-20 Paleos CM, Tsiourvas D (2003) Molecular Recognition and Hydrogen-Bonded Amphiphilies. 227 1-29... [Pg.237]

Paleos CM, Tsiourvas D (2003) Molecular Recognition and Hydrogen-Bonded Amphi-philies. 227 1-29... [Pg.265]

See other pages where Molecular recognition hydrogen bonding is mentioned: [Pg.2079]    [Pg.627]    [Pg.44]    [Pg.2693]    [Pg.2079]    [Pg.627]    [Pg.44]    [Pg.2693]    [Pg.329]    [Pg.143]    [Pg.227]    [Pg.2285]    [Pg.291]    [Pg.3]    [Pg.2834]    [Pg.66]    [Pg.175]    [Pg.179]    [Pg.182]    [Pg.182]    [Pg.188]    [Pg.191]    [Pg.200]    [Pg.62]    [Pg.59]    [Pg.167]    [Pg.173]    [Pg.1286]    [Pg.122]    [Pg.232]    [Pg.455]    [Pg.122]    [Pg.238]    [Pg.280]    [Pg.40]    [Pg.967]    [Pg.121]    [Pg.214]    [Pg.231]   
See also in sourсe #XX -- [ Pg.76 , Pg.78 ]

See also in sourсe #XX -- [ Pg.230 , Pg.232 ]



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