✦ LIBER ✦

Electrochemical studies of porphyrin redox reactions as cytochrome models

✍ Scribed by George S. Wilson

Book ID: 107946798
Publisher: Elsevier Science
Year: 1974
Tongue: English
Weight: 580 KB
Volume: 1
Category: Article
ISSN: 1567-5394
DOI: 10.1016/0302-4598(74)85018-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The reaction of cytochrome aa3 with (por

The reaction of cytochrome aa3 with (porphyrin) cytochrome c as studied by pulse radiolysis

✍ E.C.I. Veerman; J.W. Van Leeuwen; K.J.H. Van Buuren; B.F. Van Gelder 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 546 KB

Iron Porphyrins as Models of Cytochrome

Iron Porphyrins as Models of Cytochrome c Oxidase

✍ David Ricard; Maurice L'Her; Philippe Richard; Bernard Boitrel 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 167 KB

Electrochemical studies of macrocyclic c

Electrochemical studies of macrocyclic complexes as synthetic porphyrin analogs

✍ K.M. Kadish; D. Schaeper; L.A. Bottomley; M. Tsutsui; R.L. Bobsein 📂 Article 📅 1980 🏛 Elsevier Science ⚖ 453 KB

The cytochrome f–plastocyanin complex as

The cytochrome f–plastocyanin complex as a model to study transient interactions between redox proteins

✍ Isabel Cruz-Gallardo; Irene Díaz-Moreno; Antonio Díaz-Quintana; Miguel A. De la 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 999 KB

Simulation of the electrochemical behavi

Simulation of the electrochemical behavior of multi-redox systems : Current potential studies on multiheme cytochromes

✍ Cristina MORENO; António CAMPOS; Miguel TEIXEIRA; Jean LeGALL; Maria Irene MONTE 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 865 KB

Synthesis and electrochemical studies of

Synthesis and electrochemical studies of tetrathiafulvalene derivatives (TTFs) as redox active ligands

✍ Abd El-Wareth A. O. Sarhan; Makoto Murakami; Taeko Izumi 📂 Article 📅 2002 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 56 KB

## Abstract A simple route for synthesis of new tetrathiafulvalene dimethyl ester (TTF‐DME) is reported. The tetrathifulvalene dimethylester (TTF‐DME) has been prepared by introducing an ester coordination function as a bifunctional new donor. The redox behavior of the TTF‐DME was investigated in c