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Anhydrous cobalt(II) fluoride. Cobalt(II) fluoride is a chemical compound with the formula (CoF 2).It is a pink crystalline solid compound [1] [2] which is antiferromagnetic at low temperatures (T N =37.7 K) [3] The formula is given for both the red tetragonal crystal, (CoF 2), and the tetrahydrate red orthogonal crystal, (CoF 2 ·4H 2 O).
Where an acid has both a systematic and a common name (like CH 3 COOH, for example, which is known as both acetic acid and as ethanoic acid), its salts can be named from either parent name. Thus, KCH 3 CO 2 can be named as potassium acetate or as potassium ethanoate.
It is used as a solid substitute for phosgene, which is a gas and diphosgene, which is a liquid. [ 5 ] [ 6 ] Triphosgene is stable up to 200 °C. [ 7 ] Triphosgene is used in a variety of halogenation reactions.
Crystalline benzoic acid shown here is a solid and an acid, but, in the context of this article, it is not a "solid acid", which are polymeric materials and typically stronger acids. Examples of inorganic solid acids include silico-aluminates ( zeolites , alumina , silico-aluminophosphate), and sulfated zirconia .
Skeletal structural formula of Vitamin B 12.Many organic molecules are too complicated to be specified by a molecular formula.. The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are connected to one another. [1]
The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...
See: E-Z notation Violet leaf aldehyde, systematic name (E,Z)-nona-2,6-dienal, is a compound having one (E)- and one (Z)-configured double bond. The descriptors (E) (from German entgegen, 'opposite') and (Z) (from German zusammen, 'together') are used to provide a distinct description of the substitution pattern for alkenes, cumulenes or other double bond systems such as oximes.
While at University of Michigan, Omar M. Yaghi (currently at UCBerkeley) and Adrien P Cote published the first paper of COFs in 2005, reporting a series of 2D COFs. [5] They reported the design and successful synthesis of COFs by condensation reactions of phenyl diboronic acid (C 6 H 4 [B(OH) 2] 2) and hexahydroxytriphenylene (C 18 H 6 (OH) 6).