1981
DOI: 10.1107/s0108767381093628
|View full text |Cite
|
Sign up to set email alerts
|

p-Nitroaniline revisited

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

10
46
0

Year Published

1981
1981
2009
2009

Publication Types

Select...
8
1

Relationship

2
7

Authors

Journals

citations
Cited by 43 publications
(56 citation statements)
references
References 0 publications
10
46
0
Order By: Relevance
“…The mean aromatic C---C bond length of 1.377/~ is comparable to analo~gous mean distances found in the 1,4-isomer (1.388A; Driick & Littke, 1978) and in 1,2,4,5-tetracyanobenzene [1.401 (8)/~; Prout & Tickle, 1978]. The ~N bond length of 1.149 (8)/~ is typical of cyano groups and comparable to C--N distances found in various cyano derivatives (Britton, 1981a, b;Casado, Nygaard & Sorensen, 1971;Colapietro, Domenicano, Marciante & Portalone, 1981). The C---CN distance of 1.430 (7).…”
supporting
confidence: 71%
“…The mean aromatic C---C bond length of 1.377/~ is comparable to analo~gous mean distances found in the 1,4-isomer (1.388A; Driick & Littke, 1978) and in 1,2,4,5-tetracyanobenzene [1.401 (8)/~; Prout & Tickle, 1978]. The ~N bond length of 1.149 (8)/~ is typical of cyano groups and comparable to C--N distances found in various cyano derivatives (Britton, 1981a, b;Casado, Nygaard & Sorensen, 1971;Colapietro, Domenicano, Marciante & Portalone, 1981). The C---CN distance of 1.430 (7).…”
supporting
confidence: 71%
“…'s of the bond lengths and angles of the C skeleton equal to 0.007,/~ and 0.3-0.5 °, respectively. Differences as * Part IX: Colapietro, Domenicano, Marciante & Portalone (1981). large as 0.028/~ and 1.1 o occurred, however, between parameters expected to be chemically equivalent in a para-disubstituted benzene derivative.…”
Section: Introductionmentioning
confidence: 91%
“…Although the accuracy of some of the analyses is not very high, there is little doubt that the nature and electronic properties of the substituent have a definite effect on aNo 2 in the para-substituted derivatives of nitrobenzene, as they have on acooH in the para-substituted derivatives of benzoic acid Colapietro, Domenicano & Marciante, 1978). This finding supports the observation (Domenicano & Vaciago, 1976;Norrestam & Schepper, 1978) that the effect of a substituent on the internal angles of the benzene ring is not generally limited to a and fl, but may extend to y and fi as well (Fig.…”
Section: The Benzene Ringmentioning
confidence: 99%