2002
DOI: 10.1002/1521-3765(20020215)8:4<979::aid-chem979>3.0.co;2-6
|View full text |Cite
|
Sign up to set email alerts
|

Th-Symmetrical Hexakisadducts of C60 with a Densely Packed π-Donor Shell Can Act as Energy- or Electron-Transducing Systems

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
12
1

Year Published

2004
2004
2013
2013

Publication Types

Select...
7
2

Relationship

2
7

Authors

Journals

citations
Cited by 31 publications
(13 citation statements)
references
References 81 publications
0
12
1
Order By: Relevance
“…Upon the removal of THF from the organic phase on a rotary evaporator, the precipitate was collected and purified on a silica gel column with chloroform as eluent to obtain 8 as colorless powders (1.03 g, 84% yield). 1 H NMR (500 MHz, CDCl 3 ) *: 8.20~8.10 (m, 6H), 8.08 (d, J = 7.5 Hz, 4H), 8.01~7.97 (m, 6H), 7.95 (d, J = 7.5 Hz, 2H), 4.19 (t, J = 6.5 Hz, 4H), 3.39 (s, 2H), 3.29 (t, J = 7.5 Hz, 4H), 1.87~1.86 (m, 4H), 1.79~1.76 (m, 4H) ppm; 13 3073 9% 13…”
Section: Bis(pyrenebutyl) Malonate (8)mentioning
confidence: 99%
“…Upon the removal of THF from the organic phase on a rotary evaporator, the precipitate was collected and purified on a silica gel column with chloroform as eluent to obtain 8 as colorless powders (1.03 g, 84% yield). 1 H NMR (500 MHz, CDCl 3 ) *: 8.20~8.10 (m, 6H), 8.08 (d, J = 7.5 Hz, 4H), 8.01~7.97 (m, 6H), 7.95 (d, J = 7.5 Hz, 2H), 4.19 (t, J = 6.5 Hz, 4H), 3.39 (s, 2H), 3.29 (t, J = 7.5 Hz, 4H), 1.87~1.86 (m, 4H), 1.79~1.76 (m, 4H) ppm; 13 3073 9% 13…”
Section: Bis(pyrenebutyl) Malonate (8)mentioning
confidence: 99%
“…1. The figure shows a pattern of hexakis-adducts of C 60 as well as two monomers that have been synthesised experimentally by the regioselective mild Bingel reaction or tether-directed remote functionalisation [24][25][26][27]. Monomers of this type could be polymerised.…”
Section: Resultsmentioning
confidence: 99%
“…MAPS was synthesized according to the literature with little modication. 26 9,10-Bis(3-hydroxypropyloxy)anthracene (0.4 g, 1.22 mmol) and pyridine (0.1 g, 1.22 mmol) were dissolved in dry CH 2 Cl 2 (100 mL), then stearyl chloride (0.185 g, 0.61 mmol) was added dropwise to the solution under a nitrogen atmosphere. The mixture was stirred at room temperature for 2 hours.…”
Section: Modication Of Chms With Uorescent Dye Ritc (Crhms)mentioning
confidence: 99%