Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results

Journal

2009 | 7 | 1 | 138-142

Article title

Bi(NO3)3 · 5H2O mediated synthesis of 4,4′-diaminotriarylmethane leuco malachite compounds under solvent-free conditions

Content

Title variants

Languages of publication

EN

Abstracts

EN
In this report, we described the synthesis and characterization of a variety of diaminotriarylmethane derivatives with dimethylamino functional groups. These compounds were synthesized by the tandem regio-selective electrophilic aromatic substitution reaction of N,N-dimethylaniline with aryl aldehydes to form the corresponding diaminotriarylmethane compounds. In our strategy, Bi(NO3)3 was used as a catalyst under solvent free conditions to afford the desired products in good to excellent yields. [...]

Publisher

Journal

Year

Volume

7

Issue

1

Pages

138-142

Physical description

Dates

published
1 - 3 - 2009
online
23 - 12 - 2008

Contributors

  • Department of Chemistry, Payame Noor University, Qazvin Branch, Qazvin, Iran
  • School of Chemistry, University College of Science, University of Tehran, Tehran, Iran

References

  • [1] K. Venkataraman, The Chemistry of Synthetic Dyes, 1st edition (Academic Press, New York, 1952)
  • [2] H.A. Lubs, The Chemistry of Synthetic Dyes and Pigments, 1st edition (Reinhold Publishing Corporation, New York, 1955
  • [3] V.G. Witterholt, Encyclopedia of Chemical Technology, 1st edition (Wiley, New York, 1969)
  • [4] D.F. Duxbury, Chem. Rev. 93, 381 (1993) http://dx.doi.org/10.1021/cr00017a018[Crossref]
  • [5] R. Muthyala, Chemistry and Applications of Leuco Dyes, 1st edition (Kluwer Academic Publishers, New York, 2002)
  • [6] F. Dittrich, M. Scholz, German Patent DD 235 115 (1986); Chem. Abstr. 107, 112216j (1986)
  • [7] B.E. Babb, D.S. Daniel, European Patent Application EP 162 685 (1985); Chem. Abstr. 104, 105638h (1985)
  • [8] R.G. Zepp, Y.I. Skurlatov, L.F. Ritmiller, Environ. Technol. Lett. 9, 287 (1988) http://dx.doi.org/10.1080/09593338809384569[Crossref]
  • [9] S.J. Culp, F.A. Beland, J. Am. Coll. Toxicol. 15, 219 (1996) [Crossref]
  • [10] D.J. Alderman, J. Fish. Dis. 8, 289 (1985) http://dx.doi.org/10.1111/j.1365-2761.1985.tb00945.x[Crossref]
  • [11] B.P. Cho, T. Yang, L.R. Blankenship, J.D. Moody, M. Churchwell, F.A. Beland, S.J. Culp, Chem. Res. Toxicol. 16, 285 (2003) http://dx.doi.org/10.1021/tx0256679[Crossref]
  • [12] Y. Maruyama, M. Ishikawa, H. Satozono, J. Am. Chem. Soc. 118, 6257 (1996) http://dx.doi.org/10.1021/ja960024z[Crossref]
  • [13] H. Kawai, T. Nagamura, J. Photochem. Photobiol. A: Chem. 92, 105 (1995) http://dx.doi.org/10.1016/1010-6030(95)04159-1[Crossref]
  • [14] H.B. Lueck, J.L. McHale, W.D. Edwards, J. Am. Chem. Soc. 114, 2342 (1992) http://dx.doi.org/10.1021/ja00033a007[Crossref]
  • [15] M. Alvaro, H. Garcia, A. Sanjuan, M. Espla, Appl. Catal. A: Gen. 175, 105 (1998) http://dx.doi.org/10.1016/S0926-860X(98)00213-0[Crossref]
  • [16] G.E. Carl, Acta Chem. Scand. 20, 444 (1966) http://dx.doi.org/10.3891/acta.chem.scand.20-0444[Crossref]
  • [17] Z.H. Zhang, F. Yang, T.S. Li, C.G. Fu, Synth. Commun. 27, 3823 (1997) http://dx.doi.org/10.1080/00397919708007307[Crossref]
  • [18] D. Guzman-Lucero, J. Guzman, D. Likhatchev, R. Martinez-Palou, Tetrahedron Lett. 46, 1119 (2005) http://dx.doi.org/10.1016/j.tetlet.2004.12.091[Crossref]
  • [19] L.-T. An, F.-Q. Ding, J.-P. Zou, Dyes Pigm. 77, 478 (2008) http://dx.doi.org/10.1016/j.dyepig.2007.06.004[Crossref]
  • [20] E.F. Pratt, L.Q. Green, J. Am. Chem. Soc. 75, 275 (1953) http://dx.doi.org/10.1021/ja01098a007[Crossref]

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11532-008-0100-x
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.