Polycyclic Life Cycle
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Polycyclic Life Cycle
Polycyclic may refer to: * Polycyclic compound, a cyclic compound with more than one hydrocarbon loop or ring structures, including: ** Polycyclic musks ** Polycyclic aromatic hydrocarbon *** Chlorinated polycyclic aromatic hydrocarbon *** Contorted polycyclic aromatic hydrocarbon * Polycyclic group In mathematics, a polycyclic group is a solvable group that satisfies the maximal condition on subgroups (that is, every subgroup is finitely generated). Polycyclic groups are finitely presented, which makes them interesting from a computational ..., in mathematics, a solvable group that satisfies the maximal condition on subgroups * Polycyclic spawning, when an animal reproduces multiple times during its lifespan {{disambig ...
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Polycyclic Compound
In the field of organic chemistry, a polycyclic compound is an organic compound featuring several closed rings of atoms, primarily carbon. These ring substructures include cycloalkanes, aromatics, and other ring types. They come in sizes of three atoms and upward, and in combinations of linkages that include tethering (such as in biaryls), fusing (edge-to-edge, such as in anthracene and steroids), links via a single atom (such as in spiro compounds), bridged compounds, and longifolene. Though poly- literally means "many", there is some latitude in determining how many rings are required to be considered polycyclic; many smaller rings are described by specific prefixes (e.g., bicyclic, tricyclic, tetracyclic, etc.), and so while it can refer to these, the title term is used with most specificity when these alternative names and prefixes are unavailable. In general, the term polycyclic includes polycyclic aromatic compounds, including polycyclic aromatic hydrocarbons, as well as ...
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Polycyclic Musks
Synthetic musks are a class of synthetic aroma compounds to emulate the scent of deer musk and other animal musks (castoreum and civet). Synthetic musks have a clean, smooth and sweet scent lacking the fecal notes of animal musks. They are used as flavorings and fixatives in cosmetics, detergents, perfumes and foods, supplying the base note of many perfume formulas. Most musk fragrance used in perfumery today is synthetic. Synthetic musks in a narrower sense are chemicals modeled after the main odorants in animal musk: muscone in deer musk, and civetone in civet. Muscone and civetone are macrocyclic ketones. Other structurally different but functionally similar compounds also came to be known as musks. Nitro musks An artificial musk was obtained by Albert Baur in 1888 by condensing toluene with isobutyl bromide in the presence of aluminium chloride, and nitrating the product. It was discovered accidentally as a result of Baur's attempts at producing a more effective form of ...
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Polycyclic Aromatic Hydrocarbon
A polycyclic aromatic hydrocarbon (PAH) is a class of organic compounds that is composed of multiple aromatic rings. The simplest representative is naphthalene, having two aromatic rings and the three-ring compounds anthracene and phenanthrene. PAHs are uncharged, non-polar and planar. Many are colorless. Many of them are found in coal and in oil deposits, and are also produced by the combustion of organic matter—for example, in engines and incinerators or when biomass burns in forest fires. Polycyclic aromatic hydrocarbons are discussed as possible starting materials for abiotic syntheses of materials required by the earliest forms of life. Nomenclature and structure The terms polyaromatic hydrocarbon or polynuclear aromatic hydrocarbon are also used for this concept. By definition, polycyclic aromatic hydrocarbons have multiple rings, precluding benzene from being considered a PAH. Some sources, such as the US EPA and CDC, consider naphthalene to be the simplest PAH. ...
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Chlorinated Polycyclic Aromatic Hydrocarbon
Chlorinated polycyclic aromatic hydrocarbons (Cl-PAHs) are a group of compounds comprising polycyclic aromatic hydrocarbons with two or more aromatic rings and one or more chlorine atoms attached to the ring system. Cl-PAHs can be divided into two groups: chloro-substituted PAHs, which have one or more hydrogen atoms substituted by a chlorine atom, and chloro-added Cl-PAHs, which have two or more chlorine atoms added to the molecule. They are products of incomplete combustion of organic materials. They have many congeners, and the occurrences and toxicities of the congeners differ. Cl-PAHs are hydrophobic compounds and their persistence within ecosystems is due to their low water solubility. They are structurally similar to other halogenated hydrocarbons such as polychlorinated dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and polychlorinated biphenyls (PCBs). Cl-PAHs in the environment are strongly susceptible to the effects of gas/particle partitioning, seasonal sources, and c ...
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Contorted Polycyclic Aromatic Hydrocarbon
Contorted aromatics or more precisely contorted polycyclic aromatic hydrocarbons are polycyclic aromatic hydrocarbons (PAHs) in which the fused aromatic molecules deviate from the usual Plane (geometry), planarity. Introduction The comparison of structures of graphene and fullerene can help comprehend the origin of curved pi surfaces and contortion in PAHs. Both graphene and fullerene bear resemblance in having Sp hybridized, sp2 hybridized carbons however, exhibit different geometries (allotropes of carbon). The fact that fullerenes have five membered rings incorporated among six membered rings, makes them spherical whereas graphene remains planar due to the presence of exclusively all six membered rings in it. In general, the ideal C-C bond length and angle for C-C-C or C-C-H is about 1.42 Å and 2π/3 respectively whereas in corannulene structure, a five membered ring is surrounded by six membered rings contributing to non-planarity in the molecule. This leads to change in ...
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Polycyclic Group
In mathematics, a polycyclic group is a solvable group that satisfies the maximal condition on subgroups (that is, every subgroup is finitely generated). Polycyclic groups are finitely presented, which makes them interesting from a computational point of view. Terminology Equivalently, a group ''G'' is polycyclic if and only if it admits a subnormal series with cyclic factors, that is a finite set of subgroups, let's say ''G''0, ..., ''G''''n'' such that * ''G''''n'' coincides with ''G'' * ''G''0 is the trivial subgroup * ''G''''i'' is a normal subgroup of ''G''''i''+1 (for every ''i'' between 0 and ''n'' - 1) * and the quotient group ''G''''i''+1 / ''G''''i'' is a cyclic group (for every ''i'' between 0 and ''n'' - 1) A metacyclic group is a polycyclic group with ''n'' ≤ 2, or in other words an extension of a cyclic group by a cyclic group. Examples Examples of polycyclic groups include finitely generated abelian groups, finitely generated nilpotent groups, and finite solvab ...
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