Synthesis and Physical Characterization of Some New Hydrophobic Forms of the Solvatochromic N,N-Dialkyl-p-nitroanilines-Reference-Cited by-同舟云学术

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Synthesis and Physical Characterization of Some New Hydrophobic Forms of the Solvatochromic N,N-Dialkyl-p-nitroanilines

Published:2001-05-10 Issue:11 Volume:66 Page:4050-4054
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Mansour G.¹,Creedon W.¹,Dorrestein P. C.¹,Maxka J.¹,MacDonald J. C.²,Helburn R.³

Affiliation:

1. Department of Chemistry, Northern Arizona University, Box 5698, Flagstaff, Arizona 86011-5698

2. Department of Chemistry & Biochemistry, Worcester Polytechnic Institute, Worcester, Massachusetts 01601

3. Research Triangle Institute, Box 12194, Research Triangle Park, North Carolina 27709-2194 %helburn@rti.org

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0014764

Reference40 articles.

1. The solvatochromic comparison method. 6. The .pi.* scale of solvent polarities

2. The solvatochromic comparison method. I. The .beta.-scale of solvent hydrogen-bond acceptor (HBA) basicities

3. Solvatochromic shifts for some 4-nitroani- line and 4-nitrophenol derivatives as measures of relative solvent proton affinities

4. The Empirical Treatment of Solvent-Solute Interactions: 15 Years of .pi.*

5. Solvatochromic study on nitroanilines. Preferential solvation vs dielectric enrichment in binary solvent mixtures

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