Organic Functional Group Preparations 1983
DOI: 10.1016/b978-0-08-092556-1.50019-1
|View full text |Cite
|
Sign up to set email alerts
|

Diazo and Diazonium Compounds

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2004
2004
2018
2018

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 75 publications
0
1
0
Order By: Relevance
“…Coupling reaction of diazonium ion with deactivated or neutral skeleton is promoted due to the presence of a substituent with a nature of resilient electron withdrawing on diazonium ion. [13,14] pNA is one of the prominent organic chromophores. It is a member of a specific class of compounds known as "push or pull," in which an electrondonor (NH 2 group) and electron acceptor (NO 2 group) are joined through π-conjugated system (phenyl ring).…”
Section: Chromophore Formation and Chemistrymentioning
confidence: 99%
“…Coupling reaction of diazonium ion with deactivated or neutral skeleton is promoted due to the presence of a substituent with a nature of resilient electron withdrawing on diazonium ion. [13,14] pNA is one of the prominent organic chromophores. It is a member of a specific class of compounds known as "push or pull," in which an electrondonor (NH 2 group) and electron acceptor (NO 2 group) are joined through π-conjugated system (phenyl ring).…”
Section: Chromophore Formation and Chemistrymentioning
confidence: 99%