Multiple Cyclopropanations of C70. Synthesis and characterization of bis-, tris-, and tetrakis-adducts and chiroptical properties of bis-adducts with chiral addends, including a recommendation for the configurational description of fullerene derivatives w

1995 ◽  
Vol 78 (7) ◽  
pp. 1673-1704 ◽  
Author(s):  
Andreas Herrmann ◽  
Markus Rüttimann ◽  
Carlo Thilgen ◽  
François Diederich
Author(s):  
Vijayaraj Anantharaj ◽  
Jayant Bhonsle ◽  
Taizoon Canteenwala ◽  
Long Y. Chiang

RSC Advances ◽  
2018 ◽  
Vol 8 (73) ◽  
pp. 41692-41698 ◽  
Author(s):  
Edison Castro ◽  
Maira R. Cerón ◽  
Andrea Hernandez Garcia ◽  
Quentin Kim ◽  
Alvaro Etcheverry-Berríos ◽  
...  

The synthesis and characterization of a family of [60]fullerocurcuminoids obtainedviaBingel reactions is reported.


2007 ◽  
Vol 463 (1) ◽  
pp. 237/[519]-244/[526] ◽  
Author(s):  
Shunichi Aikawa ◽  
Yasuhiko Yoshida ◽  
Shinji Hatae ◽  
Satoko Nishiyama ◽  
D. Sakthi Kumar

1997 ◽  
Vol 50 (9) ◽  
pp. 939 ◽  
Author(s):  
Fang Chen ◽  
Parveen Akhtar ◽  
Leon A. P. Kane-Maguire ◽  
Gordon G. Wallace

A range of optically active pyrrole monomers have been synthesized in which a chiral sub- stituent is covalently bonded either to the pyrrole N or C3 ring position, namely (–)-(1R)-4-methyl-N-(1-phenylethyl)pyrrole-3-carboxamide, (+)-(1S)-4-methyl-N-(1-phenylethyl)pyrrole-3-carboxamide, (–)-(1R)-4-methyl-N-(1-naphthylethyl)pyrrole-3-carboxamide, (+)-(1S)-4-methyl-N-(1-naphthylethyl)pyrrole-3-carboxamide, (+)-(2S)-2-(1H-pyrrol-1-yl)propionic acid, (+)-(1S)-N-(1-phenyl-ethyl)pyrrole, and (–)-(1R)-N-(1-phenylethyl)pyrrole. Their chiroptical properties have been established by circular dichroism spectroscopy. Electropolymerization of the three N-substituted pyrrole monomers provided films of chiral conducting polymers, whose electrical and spectroscopic properties are described. Although oxidation of the C3 substituted pyrrole monomers was also facile, electrodeposition was poor and films of the associated polymers could not be obtained.


1996 ◽  
Vol 61 (6) ◽  
pp. 1904-1905 ◽  
Author(s):  
Amos B. Smith ◽  
Robert M. Strongin ◽  
Laurent Brard ◽  
George T. Furst ◽  
Joshua H. Atkins ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 31 (31) ◽  
pp. no-no
Author(s):  
Christine F. Richardson ◽  
David I. Schuster ◽  
Stephen R. Wilson

2000 ◽  
Vol 2 (8) ◽  
pp. 1011-1014 ◽  
Author(s):  
Christine F. Richardson ◽  
David I. Schuster ◽  
Stephen R. Wilson

2016 ◽  
Vol 20 (08n11) ◽  
pp. 1142-1147 ◽  
Author(s):  
Khanh Hy Le Ho ◽  
Bruno Jousselme ◽  
Stéphane Campidelli

In this work, we report on the synthesis and characterization of two fulleropyrrolidines bearing porphyrin/phthalocyanine and bis-phthalocyanine tweezers. The self-assembly properties in different solvents have been investigated by AFM and SEM. When deposited on surface from dichloromethane solutions, the fullerene derivatives formed aggregates of ca. 4–8 nm in height while hollow nanospheres with diameters of ca. 300–1000 nm are obtained from crystallization attempts.


ChemInform ◽  
2010 ◽  
Vol 27 (30) ◽  
pp. no-no
Author(s):  
A. B. III SMITH ◽  
R. M. STRONGIN ◽  
L. BRARD ◽  
G. T. FURST ◽  
J. H. ATKINS ◽  
...  

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