NMR Spectroscopy of 6-Benzylaminopurine Analogues. Part I. 15N NMR and Protonation Study

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F01%3A00004722" target="_blank" >RIV/00216224:14310/01:00004722 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

NMR Spectroscopy of 6-Benzylaminopurine Analogues. Part I. 15N NMR and Protonation Study

Original language description

Since nitrogen atom is the centre of primary interaction, 15N NMR spectroscopy is a very sensitive probe for studying the protonation and complexation processes. The 15N NMR parameters of 6-benzylaminopurine analogues were investigated by gradient inverse techniques. The proton in 4-chloro-6-benzylaminopurine (4Cl-BAP) is localised at nitrogen N-9, protons in (4Cl-BAP)+ ClO4- at nitrogens N-3, N-7 and protons in (4Cl-BAP)2+ (CF3COO-)2 at nitrogens N-3, N-7 and N-9.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

<a href="/en/project/LN00A016" target="_blank" >LN00A016: BIOMOLECULAR CENTER</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2001

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Chemické listy

ISSN

0009-2770

e-ISSN

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Volume of the periodical

95

Issue of the periodical within the volume

11

Country of publishing house

CZ - CZECH REPUBLIC

Number of pages

2

Pages from-to

760

UT code for WoS article

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EID of the result in the Scopus database

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