[1. The American Chemical Society; http://www.cas.org/]Search in Google Scholar
[2. Schroeder, G. (2011). Molecular receptors. From receptor molecules to functional materials, Wiad. Chem. 65, 1021.]Search in Google Scholar
[3. Molecular Receptors properties and applications. (2009). Ed. G. Schroeder, Cursiva, 2009, ISBN 978-83-62108-02-2.]Search in Google Scholar
[4. Chemical functionalization of surfaces for nanotechnology (2011) Ed. G. Schroeder, Cursiva, ISBN 978-83-62108-07-7.]Search in Google Scholar
[5. Heise, Ch. & Bier, F.F. (2006). Immobilization of DNA on Microarrays, Top. Curr. Chem., 261, 1, DOI: 10.1007/128_007.10.1007/128_007]Search in Google Scholar
[6. Takahashi, S. & Anzai, J. (2005). Phenylboronic Acid Monolayer-Modifi ed Electrodes Sensitive to Sugars, Langmuir 21, 5102, DOI: 10.1021/la050171n.10.1021/la050171n15896057]Search in Google Scholar
[7. Barriet, D., Yam, C.M., Shmakova, O.E., Jamison, A.C. & Lee, T.R. (2007). 4-Mercaptophenylboronic Acid SAMs on Gold: Comparison with SAMs Derived from Thiophenol, 4-Mercaptophenol, and 4-Mercaptobenzoic Acid, Langmuir 23, 8866, DOI: 10.1021/la7007733.10.1021/la700773317636994]Search in Google Scholar
[8. Baker, G.A., Desikan, R. & Thundat, T. (2008). Label-free sugar detection using phenylboronic acid-functionalized piezoresistive microcantilevers, Anal. Chem. 80, 4860, DOI: 10.1021/ ac702588b.]Search in Google Scholar
[9. Takahashi, S. & Anzai, J. (2005). Phenylboronic acid monolayer- modifi ed electrodes sensitive to sugars. Langmuir, 24, 5102, DOI: 10.1021/la050171n.10.1021/la050171n]Search in Google Scholar
[10. Boronic Acids. Preparation and Applications in Organic Synthesis and Medicine. Ed. D.G. Hall, WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2005, ISBN-13:978-3-527-30991-7.]Search in Google Scholar
[11. Adamczak-Woźniak, A. (2010). Synthesis application and stability of phenylboronic esters (pp. 59-85), In Functionalized molecules - synthesis, proporties and application, Ed. V.I. Rybachenko, Schidnyj Wydawnyczyj Dim, Donetsk, ISSN 978-966-317-076]Search in Google Scholar
[12. Adamczak-Woźniak, A. (2010). Phenylboronic compounds as molecular recognition and self-assembing agents (pp. 9-25), in Functionalized molecules - synthesis, proporties and application, Ed. V.I. Rybachenko, Schidnyj Wydawnyczyj Dim, Donetsk, ISSN 978-966-317-076.]Search in Google Scholar
[13. Spożyński, A., Adamczak-Woźniak, A. & Żubrowska, A. (2008). Interamolecular interactions in orto-aminomethylphenylboronic acids - potent sacharide receptor, (pp.75-91), In From concept to molecular receptor, Ed. V.I. Rybachenko, Schidnyj Wydawnyczyj Dim, Donetsk, ISSN 978-966-317-022-0.]Search in Google Scholar
[14. Spożyński, A., Żubrowska, A. & Adamczak-Woźniak, A. (2007). Synthesis of boronic acids-molecular receptor for sugars (pp. 51-89), In Synthetic receptors in molecullar recognition, Ed. V.I. Rybachenko, Schidnyj Wydawnyczyj Dim, Donetsk, ISSN 978-966-317-013-8.]Search in Google Scholar
[15. Schubert, U.S., Hofmeier, H., Newkome, G.R. (2006). Modern Terpyridine Chemistry, Wiley-VCH Verlag GmbH & Co.KGaA, Weinheim, ISBN-13:978-3-527-31475-1.10.1002/3527608486]Search in Google Scholar
[16. Constable, E.C. (2007). 2,2’:6’,2”-Terpyridines: From chemical obscurity to common supramolecular motifs, Chem. Soc. Rev., 36, 246, DOI: 10.1039/b601166g.10.1039/B601166G17264927]Search in Google Scholar
[17. Harris, E.K. (2010). Polymer or Macrocycle? Cobalt Complexes of Ditopic 2,2’:6’,2” - Terpyridine Ligands with Flexible Spacers, PhD thesis, University of Basel, Basel.]Search in Google Scholar
[18. Chiper, M. (2008). Advanced supramolecular assemblies based on terpyridine metal complexes: Understanding reaction parameters and designing new materials, PhD thesis, Technische Universiteit Eindhoven, 19. Hofmeier, H. & Schubert, U.S. (2004). Recent developments in the supramolecular chemistry of terpyridine-metal complexes, Chem. Soc. Rev., 30, 373, DOI: 10.1039/b400653b.10.1039/B400653B15280970]Search in Google Scholar
[20. Schubert, U.S. & Eschbaumer, C. (2002). Macromolecules containing bipyridine and terpyridine metal complexes: towards metallosupramolecular polymers, Angew. Chem. Int. Ed., 41, 2892, DOI: 10.1002/1521-3773.]Search in Google Scholar
[21. Shunmugam, R., Gabriel, G.J., Aamer, K.A., Tew, G.N. (2010). Metal-ligand-containing polymers: terpyridine as the supramolecular unit, Macromol Rapid Commun., 12, 784, DOI: 10.1002/marc.200900869.10.1002/marc.20090086921590971]Search in Google Scholar
[22. Sakamoto, R., Katagiri, S., Maeda, H. & Nishihara, H. (2013). Bis(terpyridine) metal complex wires: Excellent long- -range electron transferability and controllable intrawire redox conduction on silicon electrode, Coord. Chem. Rev., 257, 1493, DOI: org/10.1016/j.ccr.2012.08.025. ]Search in Google Scholar