The natural and synthetic quiñones in relation to the functions of plants.

  title={The natural and synthetic qui{\~n}ones in relation to the functions of plants.},
  author={G. L. Mcnew},
  journal={Bulletin of the Torrey Botanical Club},
  • G. L. Mcnew
  • Published 1950
  • Chemistry
  • Bulletin of the Torrey Botanical Club
6 Citations
Investigation on redox mechanism of 1,4-naphthoquinone by in situ FT-IR spectroelectrochemistry
Abstract The electrochemical character of 1,4-naphthoquinone (Q) in aprotic media and proton donor mixed solvent was explored by cyclic voltammetry (CV), in situ FT-IR spectroelectrochemistry, cyclicExpand
Investigation on the π-Dimer/σ-Dimer of 1,8-Dihydroxy-9,10-anthracenedione in the Process of Electrochemical Reduction by Using IR Spectroelectrochemical Cyclic Voltabsorptometry and Derivative Cyclic Voltabsorptometry
The electrochemical reduction of 1,8-dihydroxy-9,10-anthracenedione (Q) has been investigated by cyclic voltammetry (CV). Both 9,10-anthroquinone (AQ) and 1,8-methoxy-9,10-anthracenedione (DMeAQ) areExpand
IR spectroelectrochemical cyclic voltabsorptometry and derivative cyclic voltabsorptometry.
The combination of the IR CVA and DCVA spectroelectrochemical technique with theory analysis allows reconstructing the current-potential (i-E) curve for each step of electron transfer, which can help to understand the electron-transfer process. Expand
Towards a molecular-level understanding of the reactivity differences for radical anions of juglone and plumbagin: an electrochemical and spectroelectrochemical approach.
By employing cyclic voltammetry and in situ spectroelectrochemical electron spin resonance measurements, it was found that while semiquinone species generated from plumbagin are stable radical anions in DMSO solution, thespecies generated from juglone are more reactive. Expand
Comparative biochemistry of the phenolase complex.
  • H. S. Mason
  • Biology, Medicine
  • Advances in enzymology and related subjects of biochemistry
  • 1955