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Molecular construction

An important characteristic of biomolecular motion is that the different types of motion are interdependent and coupled to one another. For example, a large-scale dynamic transition cannot occur without involving several medium-scale motions, such as helix rearrangements. Medium-scale motions cannot occur without involving small-scale motions, such as side-chain movement. Finally, even side-chain motions cannot occur without the presence of the very fast atomic fluctuations, which can be viewed as the lubricant that enables the whole molecular construction to move. From the point of view of dynamic... [Pg.40]

This Part of the book could as well have been titled "Synthesis in Action" for it consists of specific multistep sequences of reactions which have been demonstrated by experiment to allow the synthesis of a variety of interesting target molecules. Graphical flowcharts for each synthesis define precisely the pathway of molecular construction in terms of individual reactions and reagents. Each synthetic sequence is accompanied by references to the original literature. [Pg.99]

Z-matrix was that it mirrors the way chemists think. Molecular construction using the Z-matrix is not particularly difficult for a small molecule, and symmetry can be readily imposed, as in my ethene example above. [Pg.244]

Molecular construction for a protein chain is just about impossible using the Z-matrix (unless you are particularly good at crossword puzzles). As 1 mentioned in Chapter 10, there are also immense practical difficulties associated with symmetric, cyclic and linear structures, and as time went by people began to question the use of the Z-matrix. [Pg.244]

Drcxlcr, K. E. (1992). Nanosysicins Molecular Machinery, Manufacturing, and Computation. New York Wiley, ten Wolde, A., ed. (1998). Nanotechnology Towards a Molecular Construction Kit. The Hague Netherlands Study Centre for Technology Trends. [Pg.813]

This article summarizes efforts undertaken towards the synthesis of the cyclo[ ]carbons, the first molecular carbon allotropes for which a rational preparative access has been worked out. Subsequently, a diversity of perethynylated molecules will be reviewed together, they compose a large molecular construction kit for acetylenic molecular scaffolding in one, two and three dimensions. Finally, progress in the construction and properties of oligomers and polymers with a poly(triacetylene) backbone, the third linearly conjugated, non-aromatic all-carbon backbone, will be reviewed. [Pg.45]

A TenWolde. Nanotechnology Towards a Molecular Construction Kit. The Hague STT,... [Pg.387]

Tejedor, D., Gonzalez-Cruz, D., Santos-Exposito, A., Marrero-Tellado, J.J., de Armas, R, Garcid-TeUado, F. (2005) Multicomponent Domino Processes Based on the Organocatalytic Generation of Conjugated Acetylides Efficient Synthetic Manifolds for Diversity-Oriented Molecular Construction. Chemistry A European Journal, 11, 3502-3510. [Pg.186]

Figure 85 Some carborane-containing molecular tools (159,160, and 161) in the molecular construction kit for the construction of carborane-containing grid-shaped polymers. Figure 85 Some carborane-containing molecular tools (159,160, and 161) in the molecular construction kit for the construction of carborane-containing grid-shaped polymers.
To conclude this brief note (for details see texts of Biochemistry) we stress that the thermodynamic efficiency of molecular motors can be quite high, approaching 100% but never reaching this thermodynamic limit see Everett and also Neilson and Crawford in References to Appendix. We must always be aware of the heat losses in any real process and this is true all the way from the simplest molecular machines to multi-molecular constructs to man-made machines. [Pg.190]

The 3D molecular constructs can be developed and modified to address characteristics of different states of the receptor molecules that relate to measurable functional characteristics such as activation, levels of constitutive activity, desensitization, and so forth (e.g., see refs. [5,7,9-13,28-35]). [Pg.239]

Despite formidable challenges, the construction of two- and three-dimensional all-carbon and carbon-rich networks has been pursued with great vigor in the past ten years.1121 Fueled by the availability of new synthetic methods, in particular Pd(0)-catalyzed cross-coupling reactions,1131 versatile molecular construction kits for perethynylated... [Pg.164]

Glycosylated porphyrins and miscellaneous products. A few other examples of functional glyco-compounds were prepared, persuing the idea that attaching a carbohydrate moiety can provide increased polarity and water solubility to another molecular construct. Many types of compounds have been prepared in this regard (Fig. 7). For example, polymerisable... [Pg.117]

Molecular Constructions, Polymers and Nanoparticles, Springer SerFluoresc (2010) 9 3-40, DOI 10.1007/978-3-642-04701-5 l, Springer-Verlag Berlin Heidelberg 2010... [Pg.3]

When I was a child, I had three toys that provided endless possibilities a set of wooden blocks, a set of Tinkertoys, and an Erector Set. These three toys had a lot in common. Each had a nnmber of distinct strnctnral elements that could be assembled in an amazing nnmber of ways to create something new and different. This has a direct analogy to the concept of assembling molecnles from atoms the atoms are the strnctnral elements and they can be hooked together to make molecular constructs in a great many ways. [Pg.49]

In the human CNS, glutamate is the most important excitatory neurotransmitter. Glycine is a major inhibitory neurotransmitter in the human CNS. Thus, these two amino acids, basic constituents of proteins, also function in other very important ways in behavior, emotion, learning, memory, and sensory perception. Nature uses its molecular constructs for more than one purpose. Among other neurotransmitters, dopamine, epinephrine, norepinephrine, and serotonin are derivatives of protein amino acids and are synthesized from them. [Pg.288]

Vesenka J, Henderson E, Marsh T (2002) In Fritzsche W (ed) Workshop on DNA-based molecular construction, Jena, Germany, May 2002. AIP Conf Proc 640 109-122... [Pg.158]

In the last ten years C—C bond formation by intramolecular C—II insertion has evolved from a laboratory curiosity to an effective tool for molecular construction. Procedures for C —C bond formation with control of relative and. in some cases, absolute configuration are now available. The greatest growth has been in the development of rhodium-catalyzed diazocarbonyl insertion reactions. The development of effective cnantioselective catalysts for this process will make it an even more valuable method for ring construction. [Pg.1146]


See other pages where Molecular construction is mentioned: [Pg.326]    [Pg.2]    [Pg.12]    [Pg.43]    [Pg.56]    [Pg.406]    [Pg.391]    [Pg.276]    [Pg.277]    [Pg.168]    [Pg.461]    [Pg.463]    [Pg.464]    [Pg.323]    [Pg.24]    [Pg.52]    [Pg.188]    [Pg.338]   
See also in sourсe #XX -- [ Pg.59 ]

See also in sourсe #XX -- [ Pg.2 , Pg.1230 ]




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Molecular-level construction

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