𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Photoinduced Dithiolation of Fullerene[60] with Dendrimer Disulfide.

✍ Scribed by Yutaka Takaguchi; Yoshiaki Katayose; Yasushi Yanagimoto; Jiro Motoyoshiya; Hiromu Aoyama; Takatsugu Wakahara; Yutaka Maeda; Takeshi Akasaka

Publisher
John Wiley and Sons
Year
2004
Weight
50 KB
Volume
35
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Photoinduced Reacti
ChemInform Abstract: Photoinduced Reaction of (60)Fullerene with Tertiary Amines: Synthesis of (60)Fulleropyrrolidines.
✍ S.-H. WU; D.-W. ZHANG; G.-W. WANG; L.-H. SHU; H.-M. WU; J.-F. XU; X.-F. LAO πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 29 KB πŸ‘ 2 views

Photoinduced Reaction of (60)Fullerene with Tertiary Amines: Synthesis of (60)Fulleropyrrolidines. -The photoinduced reaction of ( 60)fullerene (I) with tertiary amines such as (II) gives mixtures of isomeric (60)fulleropyrrolidine derivatives.

Photoinduced isomerization of allyl alco
Photoinduced isomerization of allyl alcohols to carbonyl compounds using dendrimer disulfide as catalyst
✍ Takaaki Tsuboi; Yutaka Takaguchi; Sadao Tsuboi πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 351 KB

## Abstract Allyl alcohols were isomerized to carbonyl compounds using diphenyl disulfide derivatives upon photoirradiation. Especially, dendrimer disulfide catalyzed the isomerization of allyl alcohols. Photoinduced isomerization in water was also succeeded by the use of water‐soluble dendrimer di

Functionalization of [60]fullerene by ph
Functionalization of [60]fullerene by photoinduced electron transfer (PET): Syntheses of 1-substituted 1,2-dihydro[60]fullerenes
✍ Christina Siedschlag; Heinrich Luftmann; Christian Wolff; Jochen Mattay πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 French βš– 348 KB

Fullerene is irradiated in the presence of the electron transfer sensitizer 9,10dicyanoanthracene (DCA) under cosensitization with biphenyl. The generated radical cation C6o Β°+ reacts with H-donors such as tert-butylmethyl ether, propionaldehyde and alcohols to give 1:1-edduets, the 1-substituted 1,