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・ Dibeng
・ Dibenz(a,h)anthracene
・ Dibenz(a,j)anthracene
・ Dibenzazepine
・ Dibenzepin
・ Dibenzo-1,4-dioxin
・ Dibenzo-18-crown-6
・ Dibenzocycloheptene
・ Dibenzofuran
・ Dibenzopentalene
・ Dibenzopyrenes
・ Dibenzothiazepine
・ Dibenzothiepin
・ Dibenzothiophene
・ Dibenzothiophene dihydrodiol dehydrogenase
Dibenzoylmethane
・ Dibenzoylmorphine
・ Dibenzyl ketone
・ Dibenzylideneacetone
・ Dibenzylpiperazine
・ DiBernardo
・ Dibeti
・ Dibharna
・ DiBiase
・ Dibiase
・ Dibiasi
・ Dibidale
・ Dibina
・ Dibindi
・ Dibis Dam


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Dibenzoylmethane : ウィキペディア英語版
Dibenzoylmethane

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1,3-Diphenyl-1,3-propanedione (dibenzoylmethane, DBM) is an aromatic 1,3-diketone derivative of acetylacetone (acac), where both methyl groups in acac have been substituted by phenyl groups. It is a white solid melting at 77−78 °C. Similar to acac, DBM exists in two tautomeric forms, with the keto-enol equilibrium of DBM shifting strongly towards the enol form, particularly in non-polar solvents such as benzene.〔 This is the result of the stability of the intramolecular hydrogen bond in the cis-enol form which is further resonance-stabilized by conjugation with phenyl rings. Due to its high photostability, derivatives of DBM such as avobenzone, have found applications as sunscreen products.
==References==


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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