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PMeT is a more common ob-iect of investigation than the structurally simpler PT, because the extra methyl group guarantees 0 - 0coupling and thus affords a more defined polymer. Interpretation of the lines as C=C stretching: 1470 cm-l and as thiophene ring deformation: 722 cm is based on comparison with PT (Furukawa et al., 1987) and on force field calculations (Faulques et al., 1989). The ground state of the neutral polymer was found to be aromatic, whereas the doped state is quinoid. This is a simple consequence of the formation of bipolarons, since the structure between two bipolarons is quinoid. PPy behaves very much like PT and PMeT, but has a slightly larger energy gapPITN has attracted considerable attention because of its strongly reduced gap even in the neutral state (Bredas, 1985). Since doping shifts absorption to a lower energy level, this polymer becomes highly transparent in the doped state. Assignment to vibrational modes is based on comparison to PT and benzene and on a force field analysis (Faulques et al., 1989; Wallnoefer et al., 1989a). Two types of Raman lines have been observed: a set of resonance-enhanced lines, which have been attributed to the neutral polymer, and another set of non-resonant-enhanced modes, attributed to the doped polymer. Interestingly, it was concluded from Raman experiments that the ground state of PITN is quinoid, whereas the doped state is aromatic. This experimental result was confirmed by a quantum chemical calculation (Lee and Kertesz, 1988). Thus, with respect to the ring structure, PITN behaves contrary to PT. PPV is attractive because it can be prepared as a stretch-oriented material with considerable anisotropic properties. Stretch orientation is introduced via a precursor of the polymer. The lines at 1330 and 1628 cm have been how do i print barcodes in excel 2010 Follow these 7 Steps to Install a Barcode Font in Excel + Word
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