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2012 | 10 | 5 | 1640-1646
Tytuł artykułu

Synthesis of fluorescent carboxylic acid ligands for construction of monolayers on nanostructures

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Two new long-chain carboxylic acids (1, 2) bearing strong fluorescent group pyrene as ligands for Self-Assembled Monolayers (SAMs) have been synthesized. The multistep targeted synthesis is accomplished by use of Pyren-1-yl methylamine hydrochloride and employing simplified synthetic protocols. Compound 2 contains a chiral center purposely introduced along the atom chain in order to make it suitable for chiro-optical studies of the resulting SAMs. [...]
Wydawca

Czasopismo
Rocznik
Tom
10
Numer
5
Strony
1640-1646
Opis fizyczny
Daty
wydano
2012-10-01
online
2012-07-21
Bibliografia
  • [1] S.A. Jadhav, Cent. Eur. J. Chem. 9, 369 (2011) http://dx.doi.org/10.2478/s11532-011-0024-8[Crossref]
  • [2] G.N. Allara, R.G. Nuzzo, Langmuir, 1, 45, (1985) http://dx.doi.org/10.1021/la00061a007[Crossref]
  • [3] D.L. Allara, G.N. Nuzzo, Langmuir 1, 52 (1985) http://dx.doi.org/10.1021/la00061a008[Crossref]
  • [4] C. Raimondo, M. Alloisio, A. Demartini, C. Cuniberti, G. Dellepiane, S.A. Jadhav, G. Petrillo, E. Giorgetti, C. Gellini, M. Muniz-Miranda, J. Raman Spectrosc. 40, 1831 (2009) http://dx.doi.org/10.1002/jrs.2327[Crossref]
  • [5] A. Demartini, M. Alloisio, C. Cuniberti, G. Dellepiane, S.A. Jadhav, S. Thea, E. Giorgetti, C. Gellini, M. Muniz-Miranda, J. Phys. Chem. C 113, 19475 (2009) http://dx.doi.org/10.1021/jp905787h[Crossref]
  • [6] G.G. Ting, et al., Langmuir 25, 2140 (2009) http://dx.doi.org/10.1021/la802944n[Crossref]
  • [7] M.S. Lim, et al., Langmuir 23, 2444 (2007) http://dx.doi.org/10.1021/la061914n[Crossref]
  • [8] C. Yan, M. Zharnikov, A. Golzhauser, M. Grunze, Langmuir 16, 6208 (2000) http://dx.doi.org/10.1021/la000128u[Crossref]
  • [9] T.P. Vinod, J.H. Chang, J. Kim, S.W. Rhee, Bull. Korean Chem. Soc. 29, 4 (2008)
  • [10] J. Wang, A. Sellon, J. Phys. Chem. C 113, 8895 (2009) http://dx.doi.org/10.1021/jp901842p[Crossref]
  • [11] Y.T. Tao, C.Y. Huang, D.R. Chiou, L.J. Chen, Langmuir 18, 8400 (2002) http://dx.doi.org/10.1021/la025805u[Crossref]
  • [12] J.R. Lakowicz, Topics in Fluorescence Spectroscopy, vol. 2, Principles (Plenum Press, New York, 1991)
  • [13] L. Basabe-Desmonts, D.N. Reinhoudt, M. Crego-Calama, Chem. Soc. Rev. 36, 993 (2007) http://dx.doi.org/10.1039/b609548h[Crossref]
  • [14] T. Förster, Angew Chem. Int. Ed. 8, 333 (1969) http://dx.doi.org/10.1002/anie.196903331[Crossref]
  • [15] M.A. Fox, J.K. Whitesell, A.J. McKerrow, Langmuir 14, 816 (1998) http://dx.doi.org/10.1021/la9707787[Crossref]
  • [16] M.A. Fox, W. Li, M. Wooten, A.J. McKerrow, J.K. Whitesell, Thin Solid Films 327, 477 (1998) http://dx.doi.org/10.1016/S0040-6090(98)00691-9[Crossref]
  • [17] M.Y. Lo, C. Zhen, M. Lauters, G.E. Jabbour, Sellinger, J. Am. Chem. Soc. 129, 5808 (2007) http://dx.doi.org/10.1021/ja070471m[Crossref]
  • [18] B.C. Roy, B. Chandra, D. Hromas, S. Mallik, Org. Lett. 5, 11 (2003) http://dx.doi.org/10.1021/ol026891s[Crossref]
  • [19] Organic Syntheses 2, 276 (1943)
  • [20] Organic Syntheses 19, 45 (1939)
  • [21] J.M. Khurana, S. Chauhan, G. Bansal, Monatshfte fur Chemie, 135, 83 (2004) http://dx.doi.org/10.1007/s00706-003-0114-1[Crossref]
  • [22] S.A. Jadhav, Synlett 8, 1287 (2010) and references there in. http://dx.doi.org/10.1055/s-0029-1219806[Crossref]
  • [23] T. Semeraro, C. Mugnaini, F. Manetti, S. Pasquini, F. Corelli, Tetrahedron 64, 11249 (2008) http://dx.doi.org/10.1016/j.tet.2008.09.030[Crossref]
  • [24] J. Kundo, N. Suzuki, T. Imaoka, K. Takao, A. Nikanishi, Y. Kawahara, Analytical Sci. 10, 17 (1994) http://dx.doi.org/10.2116/analsci.10.17[Crossref]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_s11532-012-0078-2
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