Examples of 'aryl rings' in a sentence

Meaning of "aryl rings"

Aryl rings: In organic chemistry, aryl rings refer to a type of ring structure with aromatic properties, such as a benzene ring. These rings often play a key role in the reactivity and stability of organic compounds

How to use "aryl rings" in a sentence

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aryl rings
The aryl rings can be substituted or unsubstituted.
Aryl groups are also referred to herein as aryl rings.
Exemplary aryl rings include phenyl or naphthyl.
Aliphatic hydrocarbyl groups can not contain aryl rings.
The aryl rings may be optionally substituted.
Since platinum catalysts are known for reduction of aryl rings.
Representative aryl rings include phenyl and naphthyl.
The ethylenically unsaturated aromatic monomer may also contain fused aryl rings.
Examples of aryl rings include phenyl and naphthalenyl.
Thus, the term includes cycloalkyl and aryl rings.
Aryl rings are monocyclic or fused bicyclic ring systems.
Examples of suitable aryl rings include phenyl and naphthyl.
The term " carbocyclic aromatic ring " includes carbocyclic rings which are also aryl rings.
Monocyclic aryl rings are also referred to as phenyl rings.
In addition, multiply substituted aryl rings are also contemplated.

See also

The aryl rings may also be substituted by annulated rings.
Examples of such monocyclic aryl rings include phenyl and biphenyl.
The aryl rings may also be substituted by additional silylsulfonates.
In addition, for example, each of the aryl rings of a naphthalene group are phenylene rings.
In certain embodiments, the two - L-CG groups are to different salicylaldehyde aryl rings.
Examples of such aryl rings include phenyl and naphthyl.
The use as claimed in claim 1, wherein a PBM comprises at least two aryl rings.
Preferable aryl rings have up to ten-members.
The use according to claim 11, wherein the SDTBM comprises at least two aryl rings.
Monocyclic aryl rings contain 6 carbon atoms in the ring.
The end groups are substituents on peripheral ( e.g., terminal ) aryl rings of the GNRs.
Functionalisation of aryl rings by deprotonation and subsequent trapping with electrophils,.
Aryl rings can have 6 or 10 carbon atoms in the ring.
Nonlimiting examples of aryl rings are phenyl, naphthyl, and the like.
Multiple aryl rings may be fused, as in naphthyl or unfused, as in biphenyl.
Some non-limiting examples of aryl rings include phenyl, naphthyl, and anthracene.
Preferred aryl rings have about 6 to about 20 ring carbons.
Non-limiting examples of such annulated aryl rings are naphthyl, tetrahydronaphthyl, phenanthryl and fluorenyl.
Preferred aryl rings include naphthyl, tolyl, xylyl, and phenyl.
And wherein the aryl rings may also be substituted by additional silylsulfonates ;.
Preferable aryl rings have five - to ten-members.
Examples of aryl rings include phenyl, naphthyl, and anthracene.
Examples of fused aryl rings include benzo, naphtho, fluoreno, and indeno.
Especially preferred aryl rings include phenyl, napthyl, anthracenyl, and phenanthrenyl.
Examples of such aryl rings include, and are not limited to, phenyl, naphthalenyl or anthracenyl.
Examples of sulfonated aryl rings ( e.g., sulfonated benzene rings ) are represented in Schemes 4 through 8.

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