Double containing structure

Star molecules containing branches made of two blocks have also been prepared by these methods102 103. Recently it was shown that such star-block copolymers exhibit very interesting so-called double-diamond structures in the bulk owing to segregation due to incompatibility between chemically unlike blocks 104. ... 

The photosynthetic apparatus in green plants and algae is located in the chloroplast, which is a flattened, double-membraned structure about 150-200 A thick/4,5 The two flat membranes lie one above the other and are united at their peripheries. These double-membraned structures have been termed thylakoids (from the Greek sacklike )/ Each membrane of the thylakoid consists of a water-insoluble lipoprotein complex which contains the light-absorbing chlorophyll and other pigments utilized in photosynthesis. 

Base pair (bp) The four nucleotides in the DNA contain the bases adenine (A), guanine (G), cytosine (C), and thymine (T). Two bases (adenine and thymine or guanine and cytosine) are held together by weak bonds to form base pairs. The two strands of human DNA are held together in the shape of a double helix by those bonds between base pairs. For example, the complementary nucleic acid base sequence to G-T-A-C that forms a double-stranded structure with the matching bases is C-A-T-G. 

A diradical is an atom or molecule containing two impaired electrons. The properties of diradicals are for the most part like those of monoradicals. They are paramagnetic and show paramagnetic resonance absorption. Although they are very reactive chemically, this is not a reliable criterion for the diradical state. Spectroscopically the diradical will probably be a triplet state if a double bond structure coupling the two electrons is geometrically possible. But when the two electrons are fairly well isolated from each other the state is probably a double doublet, like two independent radicals. 

In nature, samples usually contain different cations from those used to describe the double-layer structure Al and Fe may substitute for Si, and Fe, Fe , Mn, and Ni can all substitute for Mg to a greater or lesser degree. The substitutions may be summarized in a chemical formula written as... 

Fig. 8. Schematic representation of heteroatom-containing structural elements in polymers that are disposed for characterisation by 1H/X/Y triple resonance experiments where X = 13C and Y = 19F, 31P, 29Si, 119Sn, with possible coherence transfer pathways being indicated by single and double headed arrows.36 39 Selective observation of the correlations of the building blocks in (a)-(c) requires experiments involving out-and-back coherence transfer via Vc.h/ -A.x (a), Vc.h/ cx (b), or / . (c), whereas the simultaneous observation of all correlation signals originating from a chain of an isotope labelled sample (d) is feasible by means of a HCa(Y)-CC-TOCSY sequence.39...

This revolution in our understanding of the structure of DNA inevitably stimulated questions about its function. The double-helical structure itself clearly suggested how DNA might be copied so that the information it contains can be transmitted from one generation to the next. Clarification of how the information in DNA is converted into functional proteins came with the discovery of both messenger RNA and transfer RNA and with the deciphering of the genetic code. 

Deoxyribonucleic acid A nucleic acid containing a deoxygenated ribose sugar, having a double helical structure, and carrying genetic code in the nucleotide sequence. 

Fig. 1. Southern blot analysis of DNA showing (a) step 1, an agarose gel containing separated restriction fragments of DNA, denoted by (—), which is immersed in NaOH to denature the double-stranded structure of DNA, and then transferred by capillary flow to a nitrocellulose filter. In step 2, the bound DNA is allowed to hybridize to a labeled nucleic acid probe, and the unbound probe is washed off. In step 3, the filter is placed into contact with x-ray film resulting in (b) bands of exposure on the film which are detected after development and correspond to regions where the restriction fragment is...

X-ray diffraction studies support the double-helical structure but suggest a parallel orientation of the amylose chains.81 Since amylose has not been obtained as single crystals the diffraction data do not give a definitive answer. However, if double helices are formed by adjacent branches in amylopectin and glycogen the two strands would be parallel. Starch granules also contain amorphous starch which appears to contain single helices, possibly wrapped around lipid materials.82... 

A major feature of the spontaneous generation of a double-helical structure is that it can be employed as an organization framework, allowing the arrangement in space in a double-helical fashion of substituents attached to the bipy units. To this end, the oligo-bipy strands 137-140, containing substituents in the 4,4 position on the bipy groups, were synthesized [9.55]. 

The unit cell dimensions of all crystalline amyloses that have been determined in some detail, are listed in Table I. Also included are some intermediate forms between the va and Vjj amyloses (Ji.) and some V-amylose complexes with n-butanol, which, although not yet completely determined, have been added to illustrate the range of variability in unit cell dimensions. In the case of the Va-BuOH complex, a doubling of one unit cell axis was detected after a careful study of electron diffraction diagrams of single crystals ClO). A consequence of the doubling is that the unit cell now contains four chains, instead of the two normally found in amylose structures. Cln a strict sense, the A- and B-amyloses should also be considered as four-chain unit cells, but their double-helical structure still results in only two helices per cell) (13,1 ). 

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