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Supramolecular compounds nomenclature

Table 1 Specification/nomenclature of hosts (ligands) and suplamolecular compounds they form (decriptive terms or names of supramolecular compounds, if existing, are given m parentheses)... Table 1 Specification/nomenclature of hosts (ligands) and suplamolecular compounds they form (decriptive terms or names of supramolecular compounds, if existing, are given m parentheses)...
T0 summarize, it can be said that basic classification of supramolecular compounds has been developed using several criteria, of which the type of interaction and topological considerations are most important. On the other hand, a strict systematic nomenclature for any type of supramolecular compounds is lacking. Instead, a number of trivial names, notations, and semi-systematic names are presently in use. [Pg.272]

Classification and Nomenclature of Supramolecular Compounds, p. 261 Concave Reagents, p. 3II Cryptands, p. 334... [Pg.347]

Carbohydrates, Recognition of, p. 169 Carbonic Anhydrase Models, p. 178 Carcerands and Hernicarcerands. p. 189 Cation-n Interactions, p. 214 Cavitands, p. 219 Chiral Guest Recognition, p. 236 Classical Descriptions of Inclusion Compounds, p. 253 Classification and Nomenclature of Supramolecular Compounds, p. 261 Clathrate Hydrates, p. 274 Conzplexation of Fullerenes, p. 302 Concepts in Ciystal Engineering, p. 319 Crown Ethers, p. 326 Cryptands, p. 334 Cryptophanes, p. 340 Cyclodextrins, p. 398... [Pg.677]

Classification and Nomenclature of Supramolecular Compounds, p. 267 Clathrate Hydrates, p. 274 Crystal Growth Mechanisms, p. 364 Self-Assembly Definition and Kinetic and Thermodynamic Considerations, p. 1248 Self-Assembly in Biochemistry , p. 1257 Supramolecular Polymers, p. 1443... [Pg.802]

Classification and Nomenclature of Supramolecular Compounds, p. 261 Crown Ethers, p, 326 Cfyptands, p. 334 Hydrogen Bonding, p. 658 lonophores, p. 760 Kinetics of Complexation, p. 776 Lariat Ethers, p. 782... [Pg.987]

Fig. 2 General classification/nomenclature and descriptive terminology of host-guest supramolecular inclusion compounds... Fig. 2 General classification/nomenclature and descriptive terminology of host-guest supramolecular inclusion compounds...
The solid-state structures of these compounds are, at least at a cursory glance, dominated by OH.. . OH hydrogen bonds. Interestingly, the supramolecular chemistry of such systems can be traced back to the structure determination of 1,3-dihydroxybenzene in 1936, and Alexander Wells subsequent analysis of this structure, interpreting the topology as a utp-net (or (10,3)-d net with his own nomenclature). " ... [Pg.2389]


See other pages where Supramolecular compounds nomenclature is mentioned: [Pg.261]    [Pg.261]    [Pg.262]    [Pg.263]    [Pg.265]    [Pg.266]    [Pg.268]    [Pg.269]    [Pg.271]    [Pg.272]    [Pg.272]    [Pg.915]    [Pg.72]    [Pg.1106]    [Pg.1410]    [Pg.2170]   
See also in sourсe #XX -- [ Pg.261 , Pg.262 , Pg.263 , Pg.264 , Pg.265 , Pg.266 , Pg.267 , Pg.268 , Pg.269 , Pg.270 , Pg.271 , Pg.272 ]




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