Photochemical syntheses of fullerene-amine adducts and their characterization with1H NMR spectroscopy

Motomichi Inoue; Lorena Machi; Francisco Brown; Michiko B. Inoue; Quintus Fernando

doi:10.1016/0022-2860(94)08395-X

Photochemical syntheses of fullerene-amine adducts and their characterization with¹H NMR spectroscopy

Motomichi Inoue, Lorena Machi, Francisco Brown, Michiko B. Inoue, Quintus Fernando

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Abstract

Photoreactions of C60with aromatic or aliphatic amines in contact with air gave a new type of amine adduct with a general compound formula of C60(amine)x(OH)yOz; the amine was di-2-pyridylamine, morpholine or N,N-dimethylethylenediamine. The N,N-dimethylethylenediamine adduct was obtained as a hydrochloride. Its1H NMR spectrum showed that the adduct cation, obtained after functionalizing C60, formed an ion pair with a benzenesulfonate anion. © 1995, All rights reserved.

Original language	American English
Pages (from-to)	113-117
Number of pages	5
Journal	Journal of Molecular Structure
DOIs	https://doi.org/10.1016/0022-2860(94)08395-X
State	Published - 1 Jan 1995

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title = "Photochemical syntheses of fullerene-amine adducts and their characterization with1H NMR spectroscopy",

abstract = "Photoreactions of C60with aromatic or aliphatic amines in contact with air gave a new type of amine adduct with a general compound formula of C60(amine)x(OH)yOz; the amine was di-2-pyridylamine, morpholine or N,N-dimethylethylenediamine. The N,N-dimethylethylenediamine adduct was obtained as a hydrochloride. Its1H NMR spectrum showed that the adduct cation, obtained after functionalizing C60, formed an ion pair with a benzenesulfonate anion. {\textcopyright} 1995, All rights reserved.",

author = "Motomichi Inoue and Lorena Machi and Francisco Brown and Inoue, {Michiko B.} and Quintus Fernando",

year = "1995",

month = jan,

day = "1",

doi = "10.1016/0022-2860(94)08395-X",

language = "American English",

pages = "113--117",

journal = "Journal of Molecular Structure",

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TY - JOUR

T1 - Photochemical syntheses of fullerene-amine adducts and their characterization with1H NMR spectroscopy

AU - Inoue, Motomichi

AU - Machi, Lorena

AU - Brown, Francisco

AU - Inoue, Michiko B.

AU - Fernando, Quintus

PY - 1995/1/1

Y1 - 1995/1/1

N2 - Photoreactions of C60with aromatic or aliphatic amines in contact with air gave a new type of amine adduct with a general compound formula of C60(amine)x(OH)yOz; the amine was di-2-pyridylamine, morpholine or N,N-dimethylethylenediamine. The N,N-dimethylethylenediamine adduct was obtained as a hydrochloride. Its1H NMR spectrum showed that the adduct cation, obtained after functionalizing C60, formed an ion pair with a benzenesulfonate anion. © 1995, All rights reserved.

AB - Photoreactions of C60with aromatic or aliphatic amines in contact with air gave a new type of amine adduct with a general compound formula of C60(amine)x(OH)yOz; the amine was di-2-pyridylamine, morpholine or N,N-dimethylethylenediamine. The N,N-dimethylethylenediamine adduct was obtained as a hydrochloride. Its1H NMR spectrum showed that the adduct cation, obtained after functionalizing C60, formed an ion pair with a benzenesulfonate anion. © 1995, All rights reserved.

U2 - 10.1016/0022-2860(94)08395-X

DO - 10.1016/0022-2860(94)08395-X

M3 - Article

SN - 0022-2860

SP - 113

EP - 117

JO - Journal of Molecular Structure

JF - Journal of Molecular Structure

ER -

Photochemical syntheses of fullerene-amine adducts and their characterization with1H NMR spectroscopy

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Photochemical syntheses of fullerene-amine adducts and their characterization with¹H NMR spectroscopy