Long chain carbon molecules and diffuse interstellar lines

Nature ◽  
1979 ◽  
Vol 278 (5706) ◽  
pp. 722-723 ◽  
Author(s):  
G. F. MITCHELL ◽  
W. T. HUNTRESS
Keyword(s):  
Carbon Molecules ◽  
Long Chain

scholarly journals C2 and Diffuse Interstellar Bands

2013 ◽  
Vol 9 (S297) ◽  
pp. 121-124 ◽  
Author(s):  
M. Kaźmierczak ◽  
M. Schmidt ◽  
T. Weselak ◽  
G. Galazutdinov ◽  
J. Krełowski
Keyword(s):  
Interstellar Clouds ◽  
Physical Conditions ◽  
Diffuse Interstellar Bands ◽  
Carbon Molecules ◽  
Long Chain

AbstractC2, the simplest multicarbon molecule is a useful astronomical tool, because the analysis of its lines allows to determine the physical conditions in interstellar clouds. C2 abundances give information about the chemistry of interstellar clouds, especially on the pathway to the formation of long-chain carbon molecules, which may be connected with carriers of diffuse interstellar bands (Douglas 1977, Thorburn et al. 2003). Here we summarize all relations between C2 and diffuse interstellar bands (DIBs).

scholarly journals Formation of long-chain carbon molecules in interstellar space

1979 ◽  
Vol 66 (12) ◽  
pp. 615-615 ◽  
Author(s):  
H. D. Breuer ◽  
H. Petry
Keyword(s):  
Interstellar Space ◽  
Carbon Molecules ◽  
Long Chain

scholarly journals Long Chain Carbon Molecules in the Interstellar Medium

1980 ◽  
Vol 87 ◽  
pp. 47-58 ◽  
Author(s):  
L. W. Avery
Keyword(s):  
Interstellar Medium ◽  
The Family ◽  
Carbon Molecules ◽  
Long Chain

The long chain carbon molecules known as the cyanopolyynes (HCnN, n=3,5,7,9) are becoming increasingly more important in astrophysics. At present, the smallest member of the family, cyanoacetylene (HC3N), has been observed in at least 32 sources, and cyanodiacetylene (HC5N) in at least ten. Some 29 transitions of these two molecules have been detected to date, and the number of new sources and new lines is increasing quickly. Although the larger members of the family have not yet been found in sufficient abundance to permit studies in more than a few sources, the fact that they exist at all in detectable amounts is of interest from the standpoint of astrochemistry.

Polymer Morphology Revealed by Staining Techniques

1981 ◽  
Vol 39 ◽  
pp. 340-341
Author(s):  
A. C. Reimschuessel ◽  
V. Kramer
Keyword(s):  
Polymer Melt ◽  
Nylon 6 ◽  
Morphological Features ◽  
Negative Staining ◽  
Polymer Morphology ◽  
Crystallizable Polymer ◽  
Staining Techniques ◽  
Long Chain

Staining techniques can be used for either the identification of different polymers or for the differentiation of specific morphological domains within a given polymer. To reveal morphological features in nylon 6, we choose a technique based upon diffusion of the staining agent into accessible regions of the polymer.When a crystallizable polymer - such as nylon 6 - is cooled from the melt, lamellae form by chainfolding of the crystallizing long chain macromolecules. The regions between adjacent lamellae represent the less ordered amorphous domains into which stain can diffuse. In this process the lamellae will be “outlined” by the dense stain, giving rise to contrast comparable to that obtained by “negative” staining techniques.If the cooling of the polymer melt proceeds relatively slowly - as in molding operations - the lamellae are usually arranged in a radial manner. This morphology is referred to as spherulitic.

A theory of contamination in electron microscopes by surface diffusion

1978 ◽  
Vol 36 (1) ◽  
pp. 116-117
Author(s):  
J.T. Fourie
Keyword(s):  
Electron Beam ◽  
Surface Diffusion ◽  
High Vacuum ◽  
Ultra High Vacuum ◽  
Physical Parameters ◽  
Carbon Compounds ◽  
Hydrocarbon Molecules ◽  
Electron Microscopes ◽  
Primary Electrons ◽  
Long Chain

Contamination in electron microscopes can be a serious problem in STEM or in situations where a number of high resolution micrographs are required of the same area in TEM. In modern instruments the environment around the specimen can be made free of the hydrocarbon molecules, which are responsible for contamination, by means of either ultra-high vacuum or cryo-pumping techniques. However, these techniques are not effective against hydrocarbon molecules adsorbed on the specimen surface before or during its introduction into the microscope. The present paper is concerned with a theory of how certain physical parameters can influence the surface diffusion of these adsorbed molecules into the electron beam where they are deposited in the form of long chain carbon compounds by interaction with the primary electrons.

The effects of low-ratio n-6/n-3 PUFA on biomarkers of inflammation: a systematic review and meta-analysis

2021 ◽  
Author(s):  
Yali Wei ◽  
Yan Meng ◽  
Na Li ◽  
Qian Wang ◽  
Liyong Chen
Keyword(s):  
Systematic Review ◽  
Fatty Acid ◽  
Polyunsaturated Fatty Acid ◽  
Meta Analysis ◽  
Chain Polyunsaturated Fatty Acid ◽  
Inflammation Markers ◽  
Pufa Supplementation ◽  
Long Chain

The purpose of the systematic review and meta-analysis was to determine if low-ratio n-6/n-3 long-chain polyunsaturated fatty acid (PUFA) supplementation affects serum inflammation markers based on current studies.

Biophysics (and sociology) of ceramides.

2005 ◽  
Vol 72 ◽  
pp. 177-188 ◽  
Author(s):  
Félix M. Goñi ◽  
F-Xabier Contreras ◽  
L-Ruth Montes ◽  
Jesús Sot ◽  
Alicia Alonso
Keyword(s):  
Cell Biology ◽  
Positive Curvature ◽  
Acyl Chain ◽  
Cell Signalling ◽  
Hexagonal Structure ◽  
Lipid Monolayer ◽  
Flip Flop ◽  
Long Chain ◽  
Bilayer Permeability

In the past decade, the long-neglected ceramides (N-acylsphingosines) have become one of the most attractive lipid molecules in molecular cell biology, because of their involvement in essential structures (stratum corneum) and processes (cell signalling). Most natural ceramides have a long (16-24 C atoms) N-acyl chain, but short N-acyl chain ceramides (two to six C atoms) also exist in Nature, apart from being extensively used in experimentation, because they can be dispersed easily in water. Long-chain ceramides are among the most hydrophobic molecules in Nature, they are totally insoluble in water and they hardly mix with phospholipids in membranes, giving rise to ceramide-enriched domains. In situ enzymic generation, or external addition, of long-chain ceramides in membranes has at least three important effects: (i) the lipid monolayer tendency to adopt a negative curvature, e.g. through a transition to an inverted hexagonal structure, is increased, (ii) bilayer permeability to aqueous solutes is notoriously enhanced, and (iii) transbilayer (flip-flop) lipid motion is promoted. Short-chain ceramides mix much better with phospholipids, promote a positive curvature in lipid monolayers, and their capacities to increase bilayer permeability or transbilayer motion are very low or non-existent.

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