Modern Terpyridine Chemistry by Ulrich S. Schubert;Harald Hofmeier;George R. Newkome

By Ulrich S. Schubert;Harald Hofmeier;George R. Newkome

The 1st ebook to didactically illustrate this actual, in demand category of supramolecular building-blocks covers issues starting from terpyridine syntheses, through their chemistry and homes, supramolecular constructions, and multinuclear steel complexes, correct as much as functionalized polymers, 3D-architectures, and surfaces.Invaluable for college kids and academics in chemistry and biochemistry, fabrics scientists, in addition to polymer, advanced and physicochemists.

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A. Balavoine, Synthesis 1999, 815–820. -A. Fallahpour, M. Neuburger, M. Zehnder, Polyhedron 1999, 18, 2445–2454. 24 G. W. V. Cave, C. L. Raston, Chem. Commun. 2000, 2199–2200. 25 G. W. V. Cave, C. L. Raston, J. Chem. , Perkin Trans. 1 2001, 3258–3264. 26 G. W. V. Cave, C. L. Raston, J. L. Scotta, Chem. Commun. 2001, 2159–2169. 27 J. Uenishi, T. Tanaka, S. Wakabayashi, S. Oae, Tetrahedron Lett. 1990, 4625–4628. 28 J. E. Parks, B. E. Wagner, R. H. Holm, J. Organomet. Chem. 1973, 56, 53–66. 29 N. Miyaura, A.

Zhang, M. Zhang, Z. Lu, T. Shen, J. Mater. Chem. 1998, 8, 2055–2060. 69 M. Kimura, T. Hamakawa, K. Hanabusa, H. Shirai, N. Kobayashi, Inorg. Chem. 2001, 40, 4775–4779. 70 M. Heller, U. S. Schubert, e-polymers 2002, 27, 1–11. 71 V. Grosshenny, R. Ziessel, J. Organomet. Chem. 1993, 453, C19–C22. 72 K. Hanabusa, T. Hirata, D. Inoue, M. Kimura, H. Shirai, Coll. Surf. A: Physicochem. Eng. 2000, 169, 307–315. 73 M. L. Turonek, P. Moore, W. Errington, J. Chem. , Dalton Trans. 2000, 441–444. 74 Y. Zhang, C.

W. -K. Chung, D. -M. Ng, N. Zhu, New J. Chem. 2002, 26, 81–88. 61 W. Spahni, G. Calzaferri, Helv. Chim. Acta 1984, 67, 450–454. -A. Fallahpour, M. Neuburger, M. Zender, New J. Chem. 1999, 23, 53–61. 63 U. Siemling, U. Vorfeld, B. -G. Stammler, M. Fontani, P. Zanello, J. Org. Met. Chem. 2001, 733–737. 64 C. J. Aspley, J. A. G. Williams, New J. Chem. 2001, 25, 1136–1147. 65 E. C. Constable, M. Neuburger, A. P. Smith, M. Zehnder, Inorg. Chim. Acta 1998, 275–276, 359–365. 66 E. C. Constable, P. Harverson, D.

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