Organic molecules with large first hyperpolarisabilities (β) have attracted considerable attention over the last 20 years for their potential applications in optical data storage, telecommunications and optical signal processing. 1,2 It is already well known that molecules containing electron-donor and electron-acceptor groups linked by a large conjugated framework possess large values of β. 3 Molecular nonlinearities can be significantly enhanced by increasing the donor and acceptor strength or the length of the conjugation pathway. 4 For example, compounds 1 and 2 shown in Scheme 1, represent the highest value of µ g β 0 (510.8 × 10 -48 /esu, 800.4 × 10 -48 /esu). 5 Although significant progress has achieved in the design and syntheses of such one dimensional dipole chromophores, 6,7 in order to make a useful device, NLO chromophores must be incorporated into a fabric version, such as poled polymers, LB films, self-assembled or crystal environments, etc. Among these, chemical incorporation of chromophores into a polymer backbone is probably the most important choice. Thus the NLO chromophores that bear reactive groups and can be covalently banded into a suitable molecular structure are greatly demanded. Up to now, only a few such chromophores have