. Hz, 3 (s, Cp Ph), 130.6 (d, J(P,C) = 15.6 Hz, Co Ph), 129.1 (s, CHthienyl), ) = 8.1 Hz, Cm Ph)

P. Hz, 0 (s, CHpyridyl), 121.1 (s, CHpyridyl), 116.5 (s, CHpyridyl) (s, C=CCH2CH2) Ci Ph not observed, ) = 13.0 Hz C=CCH2CH2), p.3

F. Holmes and A. B. , 1449 (s), 1399(s), 1363(w), Chem. Rev, vol.878, issue.109, pp.3432-3030, 2009.

A. Moliton and R. C. Hiorns, Review of electronic and optical properties of semiconducting??-conjugated polymers: applications in optoelectronics, Polymer International, vol.53, issue.10, pp.1397-1412, 2004.
DOI : 10.1002/pi.1587

Y. Cheng, S. Yang, and C. Hsu, Synthesis of Conjugated Polymers for Organic Solar Cell Applications, Chemical Reviews, vol.109, issue.11, pp.5868-5923, 2009.
DOI : 10.1021/cr900182s

G. R. Whittell, M. D. Hager, U. S. Schubert, and I. Manners, Functional soft materials from metallopolymers and metallosupramolecular polymers, Nature Materials, vol.110, issue.3, pp.176-188, 2011.
DOI : 10.1038/nmat2966

A. Winter and U. S. Schubert, Synthesis and characterization of metallo-supramolecular polymers, Chem. Soc. Rev., vol.312, issue.256, pp.5311-5357, 2016.
DOI : 10.1039/C6CS00182C

J. Lehn and J. Lehn, From supramolecular chemistry towards constitutional dynamic chemistry and adaptive chemistry, Chem. Soc. Rev., vol.12, issue.July 10, pp.151-160, 2007.
DOI : 10.1039/b612035k

URL : https://hal.archives-ouvertes.fr/hal-00680548

J. R. Kumpfer and S. J. Rowan, Thermo-, Photo-, and Chemo-Responsive Shape-Memory Properties from Photo-Cross-Linked Metallo-Supramolecular Polymers, Journal of the American Chemical Society, vol.133, issue.32, pp.12866-12874, 2011.
DOI : 10.1021/ja205332w

J. M. Lehn, Dynamers: dynamic molecular and supramolecular polymers, Progress in Polymer Science, vol.30, issue.8-9, pp.814-831, 2005.
DOI : 10.1016/j.progpolymsci.2005.06.002

URL : https://hal.archives-ouvertes.fr/hal-00679766

A. Ciferri, Supramolecular Polymerizations, Macromolecular Rapid Communications, vol.23, issue.9, pp.511-529, 2002.
DOI : 10.1002/1521-3927(20020601)23:9<511::AID-MARC511>3.0.CO;2-F

H. Hofmeier and U. S. Schubert, Recent developments in the supramolecular chemistry of terpyridine???metal complexes, Chem. Soc. Rev., vol.42, issue.404, pp.373-399, 2004.
DOI : 10.1039/B400653B

A. Wild, A. Winter, F. Schlütter, and U. S. Schubert, Advances in the field of ??-conjugated 2,2???:6???,2???-terpyridines, Chem. Soc. Rev., vol.41, issue.256, pp.1459-1511, 2011.
DOI : 10.1039/C0CS00074D

S. Kelch and M. Rehahn, Synthesis and Properties in Solution of Rodlike, 2,2???:6???,2????????-Terpyridine-Based Ruthenium(II) Coordination Polymers, Macromolecules, vol.32, issue.18, pp.5818-5828, 1999.
DOI : 10.1021/ma990266u

J. Svoboda, P. ?tenclová, F. Uhlík, J. Zedník, and J. Vohlídal, Synthesis and photophysical properties of ??,??-bis(terpyridine)oligothiophenes, Tetrahedron, vol.67, issue.1, pp.75-79, 2011.
DOI : 10.1016/j.tet.2010.11.039

U. S. Schubert, H. Hofmeier, and N. G. , Modern Terpyridine Chemistry, R. a. Synth. Met, vol.96, issue.2526, pp.177-189, 1998.
DOI : 10.1002/3527608486

URL : http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.477.562

Y. Matano and H. Imahori, Design and synthesis of phosphole-based ?? systems for novel organic materials, Organic & Biomolecular Chemistry, vol.14, issue.644, pp.1258-1271, 2009.
DOI : 10.1039/b819255n

O. Fadhel, M. Gras, N. Lemaitre, V. Deborde, M. Hissler et al., Tunable Organophosphorus Dopants for Bright White Organic Light-Emitting Diodes with Simple Structures, Advanced Materials, vol.33, issue.446, pp.1261-1265, 2009.
DOI : 10.1002/adma.200801913

URL : https://hal.archives-ouvertes.fr/hal-00448206

M. Peruzzini and L. Gonsalvi, Catalysis by Metal Complexes, 2011.

L. Nyulászi, O. Hollóczki, C. Lescop, M. Hissler, and R. Réau, An aromatic???antiaromatic switch in P-heteroles. A small change in delocalisation makes a big reactivity difference, Organic & Biomolecular Chemistry, vol.105, issue.6, pp.996-998, 2006.
DOI : 10.1039/b516836h

T. Vitvarová, J. Zedník, M. Bláha, J. Vohlídal, and J. Svoboda, Effect of Ethynyl and 2-Thienyl Substituents on the Complexation of 4???-Substituted 2,2???:6???,2???-Terpyridines with Zn2+ and Fe2+ Ions, and the Spectroscopic Properties of the Ligands and Formed Complex Species, European Journal of Inorganic Chemistry, vol.62, issue.24, pp.3866-3874
DOI : 10.1002/ejic.201200256

A. P. Yang, M. Kuroda, Y. Shiraishi, and T. Kobayashi, Fluorescence from molecules and aggregates in polycrystalline thin films of ??-oligothiophenes, The Journal of Chemical Physics, vol.109, issue.19, pp.8442-8450, 1998.
DOI : 10.1063/1.477508

M. Sauer, J. Hofkens, and J. Enderlein, Basic Principles of Fluorescence Spectroscopy, 2011.
DOI : 10.1002/9783527633500.ch1

D. G. Kurth, M. Schütte, and J. Wen, Colloids Surfaces A Physicochem, Eng. Asp, pp.198-200, 2002.

C. G. Bochet, C. Piguet, and A. F. Williams, Synthesis and Electronic Properties of Intensely Coloured Iron(II) complexes with new 4-substituted planar tridentate nitrogen ligands analogous to 2, 2?: 6?, 2?-terpyridine, Helvetica Chimica Acta, vol.346, issue.1, pp.372-384, 1993.
DOI : 10.1002/hlca.19930760121

G. Zerbi, M. Gussoni, and C. Castiglioni, In Conjugated polymers, p.435, 1991.

M. Gussoni, C. Castiglioni, and G. Zerbi, In Spectroscopy of Advanced materials, 1991.

M. Zhang, P. Lu, Y. Ma, and J. Shen, Metal Ionochromic Effects of Conjugated Polymers:?? Effects of the Rigidity of Molecular Recognition Sites on Metal Ion Sensing, The Journal of Physical Chemistry B, vol.107, issue.27, pp.6535-6538, 2003.
DOI : 10.1021/jp034245k