615-94-1
Chemical Structure
2,5-Dihydroxy-1,4-benzoquinone
Synonym(s): DHBQ
- CAS No.: 615-94-1
- Formula:C6H4O4
- Molecular Weight:140.09
IUPAC Name: 2,5-dihydroxycyclohexa-2,5-diene-1,4-dione
InChIKey: QFSYADJLNBHAKO-UHFFFAOYSA-N
SMILES: O=C(C=C1O)C(O)=CC1=O
Biological Activity: 2,5-Dihydroxy-1,4-benzoquinone (DHBQ) is a redox-active quinone-based organic ligand with antibacterial activity that can be obtained from fungal metabolites. After 2,5-Dihydroxy-1,4-benzoquinone is incorporated into the Fe (dhbq) metal-organic framework, a two-electron redox process occurs, which helps improve the discharge capacity of Li+-ion battery cathodes. 2,5-Dihydroxy-1,4-benzoquinone can be used to construct conductive metal-organic frameworks suitable for Li+-ion battery cathodes[1][2].
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2,5-Dihydroxy-1,4-benzoquinone | 99.27% | 2,5-Dihydroxy-1,4-benzoquinone (DHBQ) is a redox-active quinone-based organic ligand with antibacterial activity that can be obtained from fungal metabolites. After 2,5-Dihydroxy-1,4-benzoquinone is incorporated into the Fe (dhbq) metal-organic framework, a two-electron redox process occurs, which helps improve the discharge capacity of Li+-ion battery cathodes. 2,5-Dihydroxy-1,4-benzoquinone can be used to construct conductive metal-organic frameworks suitable for Li+-ion battery cathodes. | ||||||||||||||||||||
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References
- [1]. Brewer D, et al. The antibacterial activity of some naturally occurring 2, 5-dihydroxy-l, 4-benzoquinones[J]. Canadian journal of microbiology, 1984, 30(8): 1068-1072.
- [2]. Kon K, et al. Electron-Conductive Metal-Organic Framework, Fe(dhbq)(dhbq = 2,5-Dihydroxy-1,4-benzoquinone): Coexistence of Microporosity and Solid-State Redox Activity. ACS Appl Mater Interfaces. 2021;13(32):38188-38193. [Content Brief]
