Oligomers of cyclopentadithiophene-vinylene in aromatic and quinoidal versions and redox species with intermediate forms

Quinoidal-vs.-aromatic synergy: Cyclopentadithiophene-vinylene oligomers with different sizes, in different oxidation states and as pro-aromatic quinoidals are studied considering balanced contributions of aromatic and quinoidal forms.


Introduction
Oligothiophenes (OTs) represent the prototypical molecules where, due to the weak aromaticity of thiophene, p-electron conjugation is sizeable and very appropriate for the implementation as semiconductor materials in optoelectronic applications. 1 A further modulation/improvement of p-conjugation of OTs has been achieved by intercalation with different functionalities as, for example, with vinylenes or oligothiophenevinylenes (i.e., TVs). 2 In the eld of organic electronics, where new materials with new/enhanced opto-electronic properties for device applications are desired, we here explore another combination of the thiophene/vinylene couple in which a 4,4-dihexyl-4H-cyclopenta [2,1-b:3,4-b 0 ]dithiophene (CPDT) unit replaces the thiophene in OTVs to form CPDTV oligomers. [3][4][5][6] The CPDT group has been extensively used in the construction of conducting polymers due to the excellent p-electron donor ability, ease of preparation and functionalization, large solubility by incorporation of alkyl chains at the 4-position without interference in the p-system, and complete planarization of the 12 e À fused p-dithiophene. [3][4][5][6] The CPDT unit is a versatile building block because of its electronic behavior duality: on one hand, the two cis-connected thiophenes allows CPDT to behave as an electron donor and hence it has been used in p-electron donor-acceptor conjugated copolymers. 5 CPDT-based donor-acceptor polymers have been successfully implemented in numerous device applications, such as polymeric eld-effect transistors and photovoltaics. 6 On the other hand, the central cyclopentadienyl moiety can act as an electron acceptor group, where different types of substitutions on the 4position of the CPDT unit has been explored in order to enhance the electron-withdrawing character. 6 The eld of organic electronics partially lacks the existence of reliable structure-property-function relationships on which a priori chemical designs of improved molecules and substrates could be based. Therefore, it is important to investigate the optoelectronic and structural properties of new oligomers as a function of oligomer length, (i.e., the oligomer approach), 7 which can serve as the rst step in analyzing structure-property connections for the development of new organic semiconductors. This paper utilizes this approach and outlines the investigation of the electronic and structural properties of pconjugated compounds based on the CPDT unit alternating with double bonds to create a new oligomeric series from a dimer to a hexamer (i.e., nCPDTV with n ¼ 1-6 in Scheme 1). The study is based on the X-ray solid state, electrochemical, optical (absorption and emission) and vibrational Raman characterization of their properties as a function of the oligomer size and in their neutral and charged states. The study is completed with the analysis of two versions of CPDTV, either substituted with electron-donor groups where the CPDTV core keeps a thieno-aromatic structure or with electron-acceptor groups where, conversely, the CPDTV core displays a thienoquinoidal shape.

Synthesis of nCPDTVs
The synthesis of nCPDTV oligomers was accomplished by iterative Vilsmeier bisformylation and Horner-Wadsworth-Emmons double olenation according to Scheme 1. Phosphonate derivative 2 was prepared in 92% yield by reduction of monoaldehyde 1 with sodium borohydride followed by zinc bromide-mediated Michaelis-Arbuzov reaction. Bisaldehydes 3-6 were obtained by double Vilsmeier formylation in good yields (86-93%) except for compound 5. In this case the synthesis was performed in 72% yield by using n-BuLi and DMF (see ESI †). Finally, nCPDTVs were synthesized in good yields by means of Horner-Wadsworth-Emmons reactions in the presence of potassium tert-butoxide as the base. Purication was performed using column chromatography and then recrystallization from hexane/methanol to provide the nal oligomers with high purity. The synthetic details and characterization data are collected in the ESI le (see Sections 1-3, Fig. S1-S46 †). All oligomers exhibited excellent thermal stability with decomposition temperatures around 400 C (see Fig. S47 †) Unsubstituted nCPDTVs: optical and structural properties in the neutral state Fig. 1(a) displays the electronic absorption spectra of the nCPDTV compounds in solution. These spectra show broad bands with clear vibronic structure, which progressively red-shi nearly 150 nm from 2CPDTV to 6CPDTV. Simultaneously, absorption coefficients increase in the series with increasing oligomer size. This set of wavelength peak maxima can be adjusted to a Meier's plot in order to estimate the effective conjugation length 8 (n ECL , Fig. 1(a)) from which values of n ECL ¼ 11 units and a l N ¼ 615 nm are obtainedindicating that the l max ¼ 594 nm in the hexamer is already close to the values in the ideal innite polymer. The n ECL ¼ 11 can be compared with that in OTV oligomers where n ECL ¼ 16, 2a which reects the larger p-conjugation of the CPDTV unit (14-p e À in CPDTV unit compared to and 8-p e À in TV, or 154 and 128 electrons, respectively). This longest wavelength absorption band is due to a one-electron excitation from the HOMO to the LUMO ( Fig. 1(b)). Whereas the electron density is fully delocalized over the entire backbone in smaller oligomers, this is concentrated in the middle for the longer ones without extension into the terminal rings. This aspect would justify the saturation behavior of l max for 6CPDTV.
An emission study of 2CPDTV has been carried out by measuring the uorescence spectra in solution at room temperature and at liquid nitrogen temperature ( Fig. 1(c)). The emission spectrum at room temperature is mirror-like with the absorption indicating that both originate from the same S 0 / S 1 excitation (S 1 / S 0 emission). The small Stokes shi is an indication of the small conformational reorganization upon excitation, as it is expected for a molecule with only two degrees of dihedral rotation. At 77 K, the vibronic structure is better resolved and the Stokes shi has almost vanished due to minimization of motion around the vinylene bridge. In this context, the X-ray structure of 2CPDTV-Br (i.e., 2CPDTV with two terminal bromine atoms) has been resolved and is shown in Fig. 1(d) (Fig. S48 and S49 and Table S1 †). The structure shows a highly planar p-backbone with a crystallographically symmetry-imposed torsion angle of 180 around the E-isomeric vinyl linkage, and a narrow range of Csp 2 -Csp 2 bond lengths (1.328(5)-1.455(5)Å) consistent with a high degree of p-conjugation. In addition, nearly orthogonal orientations of the hexyl side chains effectively prevent p-stacking in the solid-state.
The Raman spectra of p-conjugated molecules provide interesting insights of the p-electron delocalization in the ground electronic state. 9 These spectra for the ve molecules in solid state are displayed in Fig. 1(e) as well. Two important bands are noticed: one around 1600 cm À1 and another one around 1400 cm À1 . The 1600 cm À1 band is associated with the stretching vibration of the central C]C, or n(C]C), which displays a progressive frequency downshi of 12 cm À1 from 2CPDTV / 6CPDTV (8 cm À1 on 2CPDTV / 3CPDTV) due to a progressive enlargement of the C]C vinylene bonds upon increasing the chain length. This is a clear ngerprint of the increasing of p-electron conjugation. The most intense Raman band of the spectra appears around 1400 cm À1 and correspond to a n(C]C) of the thiophene rings of the CPDT unit. This band also experiences a frequency downshi with increasing oligomer size and this trend is consistent with other p-conjugated systems (see Fig. S50 and S51 †).

AFM morphology
A study of the surface behavior of the different nCPDTVs oligomers was performed using AFM. For these experiments CH 2 Cl 2 solutions of the 2-6CPDTV oligomers were drop-casted on HOPG. In all cases, the AFM topography images show the formation of long chains with heterogeneous height (Fig. 2, S52 and S53 †).
For most of the nCPDTV oligomers, the formation of bers was not observed when cast on other substrates like mica or SiO 2 . Only 5CPDTV shows the formation of micrometric (height and length) bers on mica. This self-assembly is driven by p-p intermolecular interactions and by the interplay with the HOPG. In this case the nearly co-planar structure of the pconjugated core offers a large available p-surface which promotes the formation of these long bers.
Unsubstituted nCPDTVs: optical and structural properties in the oxidized state Table 1 summarizes the oxidation potential values of the nCPDTVs ( Fig. S54-S63 †). While in 2CPDTV and 3CPDTV the formation of the radical cation and dication occurs in separated processes, in 4CPDTV and longer molecules the two anodic waves coalesce in one 2-electron process to yield the dication. The potential for these processes progressively decreases with the increasing molecular length indicative of enlarging p-conjugation. For 5CPDTV and 6CPDTV, higher oxidation states are also accessible.

Radical cations
The oxidation processes have been analyzed by in situ UV-Vis-NIR absorption spectroelectrochemistry and the spectra for the radical cations of all compounds are presented in Fig. 3 and Tables S2-S6 † for further details). For instance, in 3CPDTVc + , the band at 948 nm is due to the transition from the SOMO to the LUMO of the open-shell system while that at 1618 nm corresponds to the excitation from the HOMO to the SOMO (see last Section). The l max of these absorptions are represented in Fig. 3(a) as a function of 1/n where both bands t linearly, indicating that their spectral properties (e.g., wavelength, intensity, etc.) are the result of the effective extension of the p-electron structure in the radical cation state along the increasing molecular platforms (not the whole structure) when enlarging the molecular size.
The Raman spectra of the nCPDTVc + (n ¼ 3-6, that of n ¼ 2 could not be recorded) are shown in Fig. 3(b) (see Fig. S69 † for the main vibrational eigenvectors) which are characterized by a new frequency position for the vinylene n(C]C) band, appearing by nearly 30 cm À1 lower than in the neutral case. This is a clear indication that the rst one-electron oxidation greatly affects the central vinylene, due to the partial C]C / C-C transformation, or weakening, of the double bond. Changes in the frequencies of the thiophene bands are much smaller than those in the vinylene stretching band. Nonetheless, by progressing to the radical cations of the longer oligomers, the frequency of the vinylene Raman band upshis from 1564 to 1568 cm À1 on 3CPDTVc + / 4CPDTVc + due to the further dissemination of the polaronic structural defect in a larger pconjugated system. This effect reaches a plateau on 5CPDTVc + / 6CPDTVc + for which the deformation is almost constant.

Dications
Additional one-electron oxidation of the radical cation produces the progressive disappearance of the pair of radical cation bands and the continuous rise of a strong absorption at wavelengths in between the two of the radical cations. The wavelength position of the l max versus 1/n ( Fig. 3(a)) also follows a linear correlation, meaning that the dication is delocalized over larger and larger molecular dimensions. A greater slope than in the radical cations is due, in part, to the electrostatic repulsion between the charges of the same sign which pushes these further apart and contributes to more accentuated delocalization of the defects. These dication absorption bands have a high energy vibronic component which is present in all spectra and also in those of the radical cations. This reveals the stiffening of the backbone upon oxidation and is consistent with the rigidication in the vinylene bridges, as a result of the C-C]C-C / C]C-C]C evolution.
In addition, a new band appears at higher energies together with the strongest one just described. This is clearly seen in the case of 6CPDTV 2+ where, as well as the strongest band at 2121 nm, another medium intensity band at 1178 nm is detected. This double-band pattern in the dications of oligothiophenes has been associated with the presence of polaron-pair defects, where the dication, instead of being embedded in one single structural bipolaron deformation, prefers to generate two radical cation structural defects by putting away the two charges. 10,11 In order to be effective, having long molecular p-platforms, that largely minimize the repulsion, is required. This is mainly seen in oligothiophenes longer than octamers. 10,11 Clearly, 6CPDTV 2+ , thanks to its size and structure, is a candidate to stabilize the dicationic structure in a polaron-pair format rather than in a bipolaron, which is preferentially the case of the smaller oligomers, such as 3CPDTV 2+ .
The Raman spectra of the nCPDTV 2+ series (n ¼ 4-6) are displayed in Fig. 3(c). The diagnostic vinylene n(C]C) band appears at 1568 cm À1 in 4CPDTV 2+ and displays the same  frequency than the radical cation (4CPDTVc + at 1568 cm À1 ) suggesting that the perturbation of the central vinylene is similar in the dication than in the cation. This is in consonance with the repulsion effect between the charges, which pushes these towards the terminal rings. In the two longer dications, 5CPDTV 2+ and 6CPDTV 2+ , the vinylene n(C]C) bands are at almost the same values than in 4CPDTV 2+ (1567 cm À1 in both cases). The invariance of these Raman frequencies, among dications and also from the radical cations to dications of the longer oligomers, indicates that in the monovalent species, the structural alteration affects the central part of the molecule while in the divalent species these structural modications do not happen in the center but are placed at the terminal rings leaving the middle site with a partial affectation (similar to the radical cation). This spectroscopic-structural interpretation is in agreement with the formation of a polaron-pair structure in longer dications. In short, since the polaron-pair is composed of two separated radical cations, it is expected that these show similarities with the radical cations per se. 11 A polaron-pair charge defect can be described as an openshell diradical dication and can be compared, by quantum chemistry, to the bipolaron charge defect, which corresponds only to one structural deformation and therefore it is a closedshell system. Thus, we have calculated at the DFT/(U)B3LYP/6-31G** level the energy difference between the closed-and openshell structures, both as singlet states, as a function of the oligomer size for the dications and these differences, DE OC , are represented in Fig. 4(a). We observe that for 2CPDTV 2+ and 3CPDTV 2+ , DE OC ¼ 0 kcal mol À1 , indicating that the stable form is the closed-shell conguration, or bipolaron structure. From 4CPDTV 2+ , DE OC starts to be negative suggesting the preference for the open-shell form or polaron-paira preference that is more accentuated in the longer compounds.
For these dications, we have also calculated the difference between the singlet ground electronic state and the rst energy lying triplet. Following the tendency of DE OC , the triplet state is progressively getting closer to the singlet ground electronic state due to the transformation of this into an open-shell diradical. The nature and consequences on the closed-shell to open-shell transition from the data provided by quantum chemical calculations in correlation with the experimental spectroscopic data in the case of 6CPDTV 2+ is now discussed in more detail.
In Table 2 the canonical forms representing the closed-and open-shell structures (of 6CPDTVc + and of 6CPDTV 2+ from the B3LYP/6-31G** optimized structures) are represented which respectively depict a full quinoidal structure in the middle thiophenes for the radical cation and a pseudo-aromatic form for these also in the middle for the dication. In the dication, a full quinoidal structure can be formulated for the thiophene ring (closed-shell structure). However, this is unstable at the UB3LYP/6-31G** level and evolves by the rupture of one bond of this quinoidal structure giving way to the diradical species stabilized by the aromaticity recovery in the central thiophenes (aromatization of this central part is the driving force for the closed-to open-shell transition). [12][13][14] In order to probe this, we have calculated the NICS values for the rings of these oxidized species of 6CPDTV (summarized in Table 2). We see that the NICS values for the neutral species vary between À7.0 and À6.0 ppm, therefore characteristics of the thiophene aromatic rings. The formation of the radical cation produces the transformation of the central rings into quinoidal such as seen from their NICS values of À5.5 ppm. The dication, however, discloses the recovery of the NICS values in the aromatic interval around À6.0 ppm, in agreement with the formation of an open-shell diradical, which aromatizes the central part of the molecule between the radicaloid centers.

Aromatic 2CPDTV with bis(triphenylamine) substitution
Scheme 2 depicts the chemical structure of the aromatic derivative, DA(2CPDTV), disubstituted with triphenylamine groups at the terminal positions of the cyclopentadithiophenes  to study the role of the nCPDTV bridge upon charge transfer from the donor amine groups. Compound 9 was prepared in 75% yield by the Horner-Wadsworth-Emmons reaction between 7 and 8. 15 Next, the Suzuki-Miyaura cross-coupling reaction between 9 and 10 afforded DA(2CPDTV) in 66% yield (see Section 2 of ESI le for further details †). One-electron oxidation of DA(2CPDTV) yields the radical cation, DA(2CPDTV)c + , which is characterized by the appearance of two very intense bands at the expense of the bands of the neutral at 514 nm (Fig. 5(a)). These two new bands are largely red-shied to 977 and 1848 nm compared with the radical cations of 2CPDTVc + and 3CPDTVc + and very close to those of 4CPDTVc + indicating the role of the triphenylamines in extending p-conjugation.
The lowest-energy lying band at 1848 nm is predicted by TDDFT/(U)B3LP/6-31G* in DA(2CPDTV)c + at 1879 nm emerging from a HOMO / SOMO excitation where the HOMO is mainly placed at the terminal phenyl amino rings, whereas the SOMO shis the electron density mostly on the center of the dithiophene-vinylene core. The large red-shi on 2CPDTVc + / DA(2CPDTV)c + is caused by the charge resonance of the positive charge of the radical cation between the two nitrogens of the triphenyl amines through the 2CPDTV bridge during the photoinduced absorption. However, in 2CPDTVc + the charge and its corresponding excitations are placed in the center of the molecule. This band is the so-called intramolecular charge transfer band or ICT band. From its spectrum, one can infer about the type of mixed valence system involved, either class II or class III. For class III, the band might show a vibronic component and a cut-off on the low-energy side, while class II systems exhibit Gaussian-shape bands without ne structure. 16,17 From this point of view, DA(2CPDTV)c + could be described as a class II mixed valence compound where the positive charge in the ground electronic state is mainly residing in one nitrogen partially stabilized towards the bridge.
Post-oxidation of DA(2CPDTV)c + yields the dication species, DA(2CPDTV) 2+ , whose electronic absorption spectrum in Fig. 5(a) is featured by a strong band at 1254 nm which is particularly broad and is accompanied by a new band at 704 nm. These two spectral properties highlight the resemblance of this spectrum with that of 6CPDTV 2+ , due to an openshell polaron-pair dication. In this case, the great resonance stabilization of one charge in each nitrogen atom, together with the aromatization of the central dithiophenes, might justify the formation of this diradical species in this rather small compound 18-20 (see Scheme 3).

Quinoidal 2CPDTV with bis(dicyanoquinodimethane) substitution
Scheme 4 depicts the chemical structure of the quinoidal derivative of nCPDTV, Q(2CPDTV), together with its synthesis (see Section 2 of ESI le for further details †). Introduction of the dicyanomethylene moiety to 2CPDTVBr and conversion to its quinoidal form Q(2CPDTV) was accomplished using the wellestablished procedure: (i) Pd-catalyzed Takahashi coupling 21 of the malononitrile anion with the aromatic halide; (ii) further Scheme 2 Synthesis of DA(2CPDTV). Oligomers of this type are of interest as tetracyanoquinodimethanes oligothiophenes are being extensively exploited in the eld of organic conjugated molecules. 22-25 Fig. 6 displays the electrochemical response and optical absorption spectrum of Q(2CPDTV) in the neutral state; the absorption spectra of the two relevant reduced states by spectroelectrochemistry are shown in Fig. 5(b) and (d). The cyclic voltammetry of Q(2CPDTV), in contrast with 2CPDTV, shows a two-electron reduction at À0.12 V and two one-electron oxidations displaced at higher anodic potential in comparison to the aromatic analogues, at 1.10 and 1.38 V. Neutral Q(2CPDTV) shows one very strong absorption band at 744 nm with a vibronic satellite at 679 nm (ref. 26) (Fig. 5(b)). This electronic absorption spectrum is clearly similar to that of the dications of nCPDTV which exhibit the same pattern of bands (for instance in 3CPDTV 2+ has a strong peak at 1157 nm and a satellite at 1012 nm) although in the case of the charged species the absorptions are displaced at longer wavelengths indicative of the smaller HOMO-LUMO gaps. This is in accordance with a well dened closed-shell thienoquinoidal structure for Q(2CPDTV) whereas the dications display a transition between closed to open-shell structure such as discussed before.
The absorption spectra of Q(2CPDTV) as a function of the temperature in solution are shown in Fig. 6(b). Upon cooling, the progressive appearance of a new band with peak maxima at 918 nm (satellite at 798 nm) is displayed. This appears through a well resolved isosbestic point from the spectrum at room temperature, revealing the different nature of the new low temperature species of Q(2CPDTV). 27 This behavior is distinctively different from that of the aromatic nCPDTV and has been also described in other quinoidal oligothiophenes resulting from J-aggregates. 28 If aggregation takes place, it certainly overpasses the severe steric crowding by the hexyl groups at the dithiophene units revealing that the planar p-surface of the molecules promotes efficient intermolecular contacts such as in the case of the formation of bers in the neutral forms in HOPG surfaces by AFM.
UV-Vis-NIR absorption spectroelectrochemical experiments of Q(2CPDTV) have been carried out at reducing potentials. One-electron reduction gives rise to the progressive disappearance of the neutral band and the emergence of two new weak features at 1001 and 1889 nm (vibronic shoulder at 1585 nm). TDDFT/(U)B3LP/6-31G* of Q(2CPDTV)c À (Fig. 5(d)) allows the assignment of these absorptions and, in particular, the very weak band at 1889 nm is predicted at 1469 nm and is due to a double HOMO / SOMO + SOMO / LUMO promotion involving orbitals that in all cases extend or affect the whole molecule (i.e., external dicyano-methylene and the central core). Furthermore, this band is predicted to have a very low oscillator strength which is consistent with its weak absorbance in the experiment. The lowest-energy absorption band of Q(2CPDTV) c À resembles very much the ICT band of DA(2CPDTV)c + either in their wavelength positions (1848 and 1889 nm respectively) or in their shapes (both are Gaussian type bands), indicating that the radical anion is also a class II mixed valence compound in which the additional negative charge resides in the dicyanomethylene partially invading the bridge (see Scheme 3). Both bands are completely different regarding the whole absorbance: while the cation band is strong, in the anion is very weak and is probably caused by the different electron density pattern of the involved orbitals. In DA(2CPDTV)c + , the HOMO / SOMO excitation represents an electron density displacement from the external sites to the internal core, producing a large variation of the dipolar momentum (and of the transition momentum). In Q(2CPDTV)c À , the same excitation invokes a reorganization of the electron density in the whole molecule with a much smaller impact in the variation of the dipolar momentum of the transition (see Fig. 7 for the orbital topologies). Post-reduction of Q(2CPDTV)c À gives rise to the dianion species which is characterized by a band at 586 nm and is typical of those of the aromatic nCPDTV revealing the full aromatization of the bithiophene moieties upon double charging (Fig. 5(b) and (d)).
The Raman spectrum of Q(2CPDTV) in Fig. 8(a) is typical of a bipolaronic form with a quinoid structure for the thiophene and an inversion of the pattern from double to single in the central CC bond. This is reected in its vibrational Raman spectrum with the vinylene n(C]C) band at 1543 cm À1 , largely downshied relative to the values in nCPDTV at 1590 cm À1 , as a result of the weakening of the vinylene bond upon tetracyano substitution (Fig. S69 †). Therefore, the n(C]C) frequency at 1602 cm À1 in neutral 2CPDTV and at 1543 cm À1 in Q(2CPDTV) might represent the limits of a thienoquinoidization scale of the  CPDTV p-conjugated structure, the former being the frequency of the full aromatic structure (0% quinoidal, A in Fig. 8(b)) and the latter that of the full thienoquinoidal form (100% quinoidal, Q in Fig. 8(b)). In this representation, the n(C]C) bands at 1564 cm À1 for 3CPDTVc + yields a quinoidization extension of 64% in line with the aromatic / quinoidal transitional character of the radical cations. For the dications, the quinoidal percentage is almost identical (band at 1568 cm À1 in 4CPDTV 2+ results in 57% quinoidal) although the structure is not the same since the structural alteration is distributed in a polaron-pair form. Fig. 8(b) shows the wavenumber position in the quinoidal scale deduced indirectly by the n(C]C) frequency values positions regarding the values in neutral Q(CPDTV2) and 2CPDTV. These observations show how the radical cations and dications both occupy a middle region between the full aromatic and full quinoidal points revealing the transitional character of their structures. Nevertheless, the neutral oligomers logically reside in a part of the quinoidal scale, closer to the aromatic ngerprint.

Conclusions
A new series of p-conjugated oligomers based on the 4,4 0 dihexyl-4H-cyclopenta[2,1-b:3,4-b 0 ]dithiophene vinylene repeating units has been prepared and characterized by spectroscopic and modelling methods. The neutral compounds display sizeable p-conjugation with increasing molecular size and a longer mean conjugation length than their oligothiophene and oligothiophene vinylenes homologues. Consequently the new compounds show rich redox chemistry with the stabilization of polycationic states of which the radical cations and dications are strong NIR absorbersthe latter displaying singlet diradicaloid states due to the gaining or recovery of aromaticity in the thiophene rings from the unstable quinoidal bipolaronic structures. Radical cations are described as having a quinoidal structure placed in the molecular center and anked by two aromatic structures in the terminal parts. Conversely, the dications, as a result of their diradical character, display the reversed trend with aromatic segments in the molecular center surrounded by two quinoidal external moieties.
To better investigate the potential charge transport properties as channels for either positive (i.e., hole) or negative (i.e., electron) transport, two more derivatives were prepared. The CPDTV cores were substituted, either with electron donor triphenyl amino groups or with bis(dicyano-methylene) caps, enforcing a quinoidal structure in the dithiophene-vinylene bridge. The positive charge of the radical cation of the triarylamine compound is localized in the amine groups, and behave as class II mixed valence systems. The radical anion of the tetracyano compound, meanwhile has the same connement effect of the charge in the environment of the electron accepting groups. The dication and dianion of these two compounds are open-shell biradical or polaron pair and closed-shell or bipolaronic structures respectively.
The rich redox chemistry using these bridging groups, together with the adequate substitution of these cores, produce p-conjugated compounds with a variety of structures and properties. They can be exploited to function as materials for organic electronics but these materials are also of importance to gain insights into the intricate electronic structure of highly pelectron conjugated molecules.

Conflicts of interest
There are no conicts to declare.