Molecular self-assembly definition

Fluorescence Sensing of Anions, p. 566 Guanidium-Based Anion Receptors, p. (575 Halogen Bonding, p. 628 Macrocyclic Synthesis, p. 830 Molecular Squares, Boxes, and Cubes, p. 909 Naked Anion Effect, p. 939 Organometallic Anion Receptors, p. 1006 Rotaxanes and Pseudorotaxanes, p. 1194 Self-Assembly Definition and Kinetic and Thermodynamic Considerations, p. 1248 The Template Effect, p. 1493... 

Hemoglobins O2 Uptake and Transport, p. 636 Molecular Logic Gates, p. 893 Molecular-Level Machines, p. 931 Phthalocyanines, p. 1069 71—71 Stacking Theory and Scope, p. 1076 Potphyrin-Based Clathrates, p. 1150 Self-Assembly Definition and Kinetic and Thermodynamic Considerations, p. 1248 Self-Assembly Terminology, p. 1263 Strict Self-Assembly and Self-Assembly with Covalent Modifications, p. 1372 Supramolecular Photochemistry, p. 1434 Vitamin 8/2 and Heme Models, p. 1569... 

Chemical Topology, p. 229 Molecular Squares, Boxes, and Cubes, p. 909 Self-Assembly Definition and Kinetic and Thermodynamic Considerations, p. 1248 Self-Assembly Terminology, p. 1263... 

Classical Descriptions of Inclusion Compounds, p. 253 Clathrate Hydrates, p. 274 Concepts in Crystal Engineering, p. 319 Crown Ethers, p. 326 Cryptands, p. 334 DNA Nanotechnology, p. 475 Enzyme Mimics, p. 546 The Lock and Key Principle, p. 809 Molecular-level Machines, p. 931 Selectivity Thermodynamic and Kinetic, p. 1225 Self-Assembly Definition and Kinetic and Thermodynamic Considerations, p. 1248 Self-Assembly Terminology, p. 1263 Soft and Smart Materials, p. 1302 Spherands, p. 1344... 

Self-assembled monolayers (SAMs) are molecular layers tliat fonn spontaneously upon adsorjDtion by immersing a substrate into a dilute solution of tire surface-active material in an organic solvent [115]. This is probably tire most comprehensive definition and includes compounds tliat adsorb spontaneously but are neither specifically bonded to tire substrate nor have intennolecular interactions which force tire molecules to organize tliemselves in tire sense tliat a defined orientation is adopted. Some polymers, for example, belong to tliis class. They might be attached to tire substrate via weak van der Waals interactions only. 

As the analytical, synthetic, and physical characterization techniques of the chemical sciences have advanced, the scale of material control moves to smaller sizes. Nanoscience is the examination of objects—particles, liquid droplets, crystals, fibers—with sizes that are larger than molecules but smaller than structures commonly prepared by photolithographic microfabrication. The definition of nanomaterials is neither sharp nor easy, nor need it be. Single molecules can be considered components of nanosystems (and are considered as such in fields such as molecular electronics and molecular motors). So can objects that have dimensions of >100 nm, even though such objects can be fabricated—albeit with substantial technical difficulty—by photolithography. We will define (somewhat arbitrarily) nanoscience as the study of the preparation, characterization, and use of substances having dimensions in the range of 1 to 100 nm. Many types of chemical systems, such as self-assembled monolayers (with only one dimension small) or carbon nanotubes (buckytubes) (with two dimensions small), are considered nanosystems. 

Liquid crystals (LCs) are molecules that have the ability to self-assemble into organized mesophases with properties intermediate between those of crystalline solids and isotropic liquids [1,2]. In LC phases, the molecules are dynamic and collectively behave as a viscous liquid but retain on average a degree of organization reminiscent of an ordered, crystalline solid. Consequently, they can be considered ordered fluids, as a more accurate definition. LCs can be subdivided into two general classes—thermotropic LCs and lyotropic LCs—depending on the environmental and molecular factors that govern how they form ordered fluid phases. 

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