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・ Chloramine
・ Chloramine-T
・ Chloramphenicol
・ Chloramphenicol acetyltransferase
・ Chloramphenicol phosphotransferase-like protein family
・ Chlorane Bar attack
・ Chlorangiellaceae
・ Chloranil
・ Chloranilic acid
・ Chloranthaceae
・ Chlorarachniophyte
・ Chlorargyrite
・ Chloraseptic
・ Chloraspilates
・ Chlorastrolite
Chlorate
・ Chlorate reductase
・ Chlorbenside
・ Chlorbenzoxamine
・ Chlorbisan
・ Chlorcyclizine
・ Chlordane
・ Chlordecone reductase
・ Chlordiazepoxide
・ Chlordiazepoxide/clidinium bromide
・ Chlordimeform
・ Chlorella
・ Chlorella autotrophica
・ Chlorella pyrenoidosa
・ Chlorella sorokiniana


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Chlorate : ウィキペディア英語版
Chlorate

The chlorate anion has the formula ClO3. In this case, the chlorine atom is in the +5 oxidation state. "Chlorate" can also refer to chemical compounds containing this anion; chlorates are the salts of chloric acid. "Chlorate", when followed by a Roman numeral in parentheses, e.g. chlorate(VII), refers to a particular oxyanion of chlorine.
As predicted by VSEPR, chlorate anions have trigonal pyramidal structures.
Chlorates are powerful oxidizers and should be kept away from organics or easily oxidized materials. Mixtures of chlorate salts with virtually any combustible material (sugar, sawdust, charcoal, organic solvents, metals, etc.) will readily deflagrate. Chlorates were once widely used in pyrotechnics for this reason, though their use has fallen due to their instability. Most pyrotechnic applications that formerly used chlorates now use the more stable perchlorates instead.
==Structure and bonding==
The chlorate ion cannot be satisfactorily represented by just one Lewis structure, since all the Cl-O bonds are the same length (1.49 Å in potassium chlorate), and the chlorine atom is hypervalent. Instead, it is often thought of as a hybrid of multiple resonance structures:

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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