Diindeno[1,2-b:2′,1′-n]perylene: a closed shell related Chichibabin's hydrocarbon, the synthesis, molecular packing, electronic and charge transport properties

A fixed Chichibabin's hydrocarbon CHI1 shows a closed shell configuration with a broad absorption from 400 up to 900 nm.


Introduction
The design and synthesis of new functional p-conjugated materials is a major issue for the development of the next generation of organic optoelectronic devices. Continuous research efforts have contributed to the great advances in the development of materials, along with innovations and optimizations of the device structure and processing. 1,2 The progresses made are the result of the improvements in the fabrication processes and a better understanding of the design rules, yielding efficient p-conjugated materials. Tremendous efforts have been focused on the functionalization of known molecules (e.g. thiophene, benzene, uorene, etc.) with electron-withdrawing or donating groups, alternating electron donors and electron decient building blocks or the incorporation of heteroatoms into the p-conjugated backbone. 3 However, further improvement of the material performance requires the development of a new concept in the designing of building blocks and an in-depth understanding of the structure-property relationships. Toward this end, several synthetic approaches have been developed, with a promising one being the use of quinoidal molecules as a useful building block for constructing functional materials. Quinoidal polycyclic hydrocarbons (QPHs) have recently been the subject of intense research due to their potential to have an open shell character with fascinating optical, electronic and magnetic properties. 4 Environmentally stable closed shell QPHs are very promising for OFETs and photovoltaic applications due to their inherent planar structure that could improve the p-p stacking capability and facilitate charge delocalization and transport. Moreover, the quinoidal p-conjugated system reduces the HOMO-LUMO energy gap by stabilizing the LUMO energy level more than it destabilizes the HOMO level compared to the aromatic analogues and shows amphoteric redox behaviours, which is a prerequisite for their use as ambipolar semiconductors. Several QPHs have been developed in recent years, such as bisphenalenyls, 5 zethrenes 6 and indenouorenes. 7 The latter family is of interest due to the ease of their synthesis and the tuning of their optical and electronic properties, with the possibility to fuse two indene units in different fashions into a diverse p-conjugated spacer. Considering a benzene group as the conjugated spacer, four isomers with a plane or centre of symmetry have been developed (Fig. 1). 7a-d,f They have either a central para-(1a, 1c), ortho-(1b) or metha-quinomethane (1d) unit. Isomers 1a-c are best described as quinoidal closed shell molecules in the ground state, ensuring a good stability, whereas 1d only has a little contribution of the singlet biradical canonical structure to the ground-state electronic conguration. The difference between these isomers is best described by considering the number of aromatic sextets between the quinoidal form (closed shell) and the biradical form (open shell) according to Clar's rule. The closed shell 1a-c has two aromatic sextets whereas the corresponding open shell has three aromatic sextets. The gain in aromaticity in the corresponding open shell resonance is not enough to compensate the dissociation energy of the two double bonds and the reorganization of the p-electrons in the system. For 1d, the biradical form has two more aromatic sextets compared to the quinoidal one and leads to a little contribution from the biradical resonance in the ground state. The biradical character of molecules belonging to the bisindeno-acene family can be simply anticipated when a difference of at least two aromatic benzenoid sextets between the quinoidal and biradical form is present.
Despite the progress made on synthesizing indenouorene materials with good optical and electronic properties, only three reports describing the organic eld effect transistor (OFET) characteristics have been reported. Low carrier mobilities (hole and electron) of 8.2 Â 10 À6 cm 2 V À1 s À1 were measured for arylsubstituted derivatives in evaporated thin lms. 7b The low mobilities were attributed to the lack of efficient p-p stacking in the crystal. A higher hole mobility (1.6 Â 10 À2 cm 2 V À1 s À1 ) was obtained from a preliminary eld effect transistor test on the spin-coated thin lms of a diindenothienothiophene derivative. 7h Single crystal-OFETs with hole and electron mobilities up to 7 Â 10 À4 and 3 Â 10 À3 cm 2 V À1 s À1 , respectively, were reported too. 7c However, single crystal devices might be not well suited for practical applications in large area electronics due to their processing limitations.
In an effort to gain a deeper insight into the electronic structure of the indenoacene family and to further expand their versatility scaffold, we are interested in other conjugated systems that are larger than previously reported. Thus, from the viewpoint of molecular design, we introduce indeno groups into the perylene scaffold for several reasons: (a) the diindeno[1,2b:2 0 ,1 0 -n]perylene CHI1 (Fig. 1) can be regarded as a xed Chichibabin's hydrocarbon CHI2, which was recently found to exist in a semi-quinoid structure, with a signicant contribution of the singlet biradical resonance form (Fig. 1). 8 Moreover, two recent tetrabenzo-Chichibabin's derivatives have been disclosed, displaying either a closed (CHI3) or an open shell (CHI4) electronic conguration (Fig. 1). 9 For these cases, even though the closed shell form has two more aromatic sextets than the open shell one, the electronic conguration could be tuned by a substituent effect on the thermodynamic stabilization of the biradical form. CHI1 can be viewed also as an extension of the closed shell indeno[2,1-c]uorene 1c derivative in which the central phenylene group is replaced by a p-biphenylene linker. Therefore, the extension of the p-conjugation should lead to a low band gap material; (b) according to Clar's rule, the quinoidal structure of CHI1 and the biradical resonance form have the same number of aromatic sextets (Fig. 1). So, in line with the relationship between the structure and the electronic conguration known for the indenouorene family as described above, CHI1 should have a closed shell conguration ensuring a good stability. Thus, it is of high interest to assess the electronic conguration of CHI1 in order to a have better understanding of the relationship between the structure and the electronic conguration; (c) the perylene scaffold should promote good p-p overlap, thus good charge transport properties could be expected.
Herein, we describe an efficient synthetic method to prepare CHI1, in which the conjugation of the central perylene core is extended by the annelation of the two indene units. To address the processability issue, we introduce the (triisopropylsilyl) acetylene group to both improve the solvent solubility, stabilizing the structure by an electronic effect, increase the p-p interactions and improve the charge transport properties. 10 An overview of the synthetic procedures is presented rst and then the electronic and electrical properties of these new materials, including their absorption, electrochemical properties, molecular packing and charge transport behaviour, are developed and discussed.

Results and discussions
The synthetic path used to synthesize CHI1 followed the same strategy as the synthesis of indenouorene derivatives which relies on the synthesis of a diketone molecule that is consequently reacted with an appropriate lithium derivative, followed by a dehydroxylation reaction (Scheme 1). However, the preparation of CHI1 was more challenging than that of the other indenoacene derivatives reported so far due to the need to construct the perylene core with suitable functionalities. One of the simplest and efficient methodologies to construct the perylene moiety is based on a base-promoted cyclodehydrogenation reaction of the 1,1 0 -binaphthyl derivatives bearing withdrawing substituents at the peri-position using K 2 CO 3 and ethanolamine. 11,12 We assumed that this procedure should work well with the ketone groups positioned in para of the reactive carbons in which the cyclisation occurs. Consequently, the critical reaction involved the preparation of the diindeno[1,2-b:2 0 ,1 0 -n]perylene-5,12-dione 7 from the 1,1 0 -binaphthyl derivative 6, namely 11H, The synthesis starts with the dimerization of 6-methoxytetralone using zinc in presence of protic chlorotrimethylsilane. 13 It should be noted that with a simple ltration under a silica gel pad, the 6,6 0 -dimethoxy-3,3 0 ,4,4 0 -tetrahydro-1,1 0 -binaphthalene 1 decomposes partially to the corresponding hexahydrobenzo[j]uoranthene derivative involving a ring closure with the formation of 5-membered ring. Nevertheless, compound 1 was isolated with a good quality and a yield of 86% aer workup without purication. The aromatisation of compound 1 could not be carried out with a classical oxidant such DDQ and p-chloranil. Thus, the 6,6 0 -dimethoxy-1,1 0binaphthalene 2 was obtained in 59% yield using trityl uoroborate instead. Treatment of 2 with BBr 3 quantitatively yielded the corresponding dihydroxybinaphthalene 3, followed by a triation reaction carried out in a classical manner which afforded the corresponding 1,1 0 -binaphthalene triate 4. The palladium-catalysed Suzuki-Miyaura cross-coupling reaction between the bis-triate 4 and 2-methoxycarbonylphenylboronic acid gave compound 5 in a 66% yield. The cyclization of the ester group was carried out with methanesulfonic acid to furnish the dione 6 in a quantitative yield. The cyclodehydrogenation of 6 was efficiently done with K 2 CO 3 /ethanolamine upon heating to give the desired parent diindenoperylene-5,12-dione 7. The addition of the lithiumtriisopropylsilylacetylene to 7 induced the formation of the diols 8 in excellent yield. The corresponding syn-/anti-diastereoisomers were easily separated under column chromatography as the difference in the retention factor (R f ) is large. The R f values were found to be 0.39 and 0.09 in a mixture of petroleum ether/ dichloromethane for the rst and second diastereoisomer respectively. The SnCl 2 -mediated dehydroxylation of the resulting mixture of diols was carried out in toluene at 120 C for 1 h, leading to a dark blue solution. A longer time induces the formation of by-products. The target molecule CHI1 was isolated in a 66% yield over two steps aer purication under a silica gel column in a mixture of toluene/petroleum ether (50/50). Due to the very low solubility of compounds 6 and 7 in common solvents, only the 1 H NMR spectrum of 7 could be recorded. However, these two molecules were characterized by infrared spectroscopy, X-ray crystallography and elemental analysis. 14,15 Infrared spectra of compounds 7 and 8 showed the characteristic peaks of C]O stretching belonging to an arylketone at 1695 cm À1 and 1691 cm À1 , respectively (see ESI †). Other signals related to the formation of a H-bonded carbonyl group structure are detected at 1601 cm À1 and 1579 cm À1 for 7 and 1605 cm À1 and 1579 cm À1 for 8. The target molecule CHI1 was fairly soluble in common organic solvents and was characterized by 1 H NMR, infrared spectroscopy, elemental analysis and X-ray crystallography (see ESI †). 16 The 1 H NMR spectrum of CHI1 shows a sharp signal at room temperature and consequently supports the quinoidal structure of the ground state (see ESI †). Crystals suitable for X-ray structure analysis were obtained by recrystallization from chloroform for 7 and benzene for CHI1 (Fig. 2). Both compounds gave crystals with an orthorhombic symmetry. 7 and CHI1 crystallize in the Pbcn and Pbca space groups, respectively. It should be noted that CHI1 co-crystallized with benzene molecules in a ratio 2 to 1. Selected bond lengths of the p-part, which changes signicantly between 7 and CHI1, are listed in Table 1 together with those of Chichibabin's molecules CHI2 and CHI3.
For comparison, the theoretical bond lengths of 7 and CHI1 without the TIPS groups estimated by the DFT calculations are given in Table 1 as well. The calculated bond lengths for both molecules agree well with those of the experimental data within experimental errors. The crystal structure of 7 shows characteristics of the perylene scaffold. By contrast, the structure of CHI1 shows clearly a bond-length alternation in the p-skeleton: the bonds denoted by a, c, and e have substantial double-bond character, whereas the bonds denoted by b, d and f-i have more of a single-bond character ( Table 1; Scheme 1). The bonds lengths (d, e, h, i) of the ve-membered rings are typical for the closed shell quinoidal indenouorene derivatives. The shortening of bond length a (1.406 (5)Å) compared to bond lengths a 0 (1.470 (5)Å) and a (1.448 (4)Å) in the corresponding Chichibabin's molecule CHI2 is signicant but longer than the one observed for CHI3 (1.350 (8)Å). The bond length of a in CHI1 is longer than a typical double bond, which is ascribed to steric hindrance between the two hydrogens located in the bay region of the perylene core. The distance between them is less than the sum of their van der Waals radii. The bond lengths suggest unambiguously that CHI1 has a quinoidal electronic conguration in the ground state. It should be noted that CHI1 is stable in a non-degassed toluene solution for more than six months in the dark and for 1 week in the laboratory environment. Moreover, the analysis of the nucleus independent chemical shi (NICS) values, NICS(1) (NICS(1)zz), 18 for the ve-membered and the quinoidal adjacent rings were À1.80 (5.25) and À1.66 (4.04), respectively, indicates a weak antiaromatic character. In comparison, the isomer 1c shows a stronger antiaromatic character, with values for the ve-membered ring of 4.18 (21.76) and 0.57 (9.61), for the quinoidal ring (see ESI †).
Compounds, 7 and CHI1, arrange into a 1-D columnar stack in which the molecules form pairwise slipped stacks. The distance between the average planes within the pair is 3.37Å and 3.39Å and 3.19Å and 3.41Å within adjacent pairs for 7 and CHI1 respectively. The lateral slip of the p-conjugated system was found to be 1.56Å and 2.04Å in the pair and 5.14Å and 2.00Å between pairs for 7 and CHI1 respectively. In 7, the 1Dcolumns form layers of parallel columns and each alternate layer is twisted to each other. The dihedral angle between the average planes is 54.28 . The 1D-columns interact through hydrogen bonds (CH-O) of length 2.47Å into the layers and 2.43Å within the layers. For CHI1, the 1D-columns are separated from the adjacent columns by the TIPS groups and benzene molecules.
The charge-transfer processes are impacted by the geometry and molecular packing as well as by the intermolecular electronic coupling. An accurate understanding of all these molecular characteristics is an important prerequisite for the design and selection of appropriate molecules, as well as for optimizing the performance of the devices. Therefore, we have performed a study of the transfer integral in the dimers of 7 and CHI1 (Fig. S2 in ESI †) using the Amsterdam Density Functional (ADF) program package. Compound 7 exhibits a large intradimer transfer integral, of the order of 142 meV and 4.3 meV for inter-dimer contacts. Although compound CHI1 displays a slightly different crystalline structure, the calculated transfer integral (5.4 meV) is much lower than the transfer integral of 7. Hence, this study of the transfer integral shows clearly that the intra-columnar direction is a favourable direction for charge transport.
The UV-visible absorption spectra of 7 and CHI1 are depicted in Fig. 3. Compound 7 was very insoluble in common solvents, even at a concentration of 2 Â 10 À5 mol L À1 . At this concentration, the spectrum shows a maximum wavelength at 592 nm and a diffusion band indicating the presence of aggregates. Compound CHI1 displays a strong blue colour in a toluene solution. The UV-vis spectrum of CHI1 exhibits strong acene-like vibronic features in the visible energy range that extends into the near-IR region (900 nm), with a lower energy of l max at 683 nm.
Cyclic voltammetry and square wave voltammetry (SQW) were used to investigate the electrochemical behaviour and probe the HOMO/LUMO levels of CHI1 (Fig. 4). The compound CHI1 showed an amphoteric redox behaviour and exhibits two reversible oxidation and reduction peaks, which are typical for Fig. 4 Square wave voltammogram of CHI1 in a dichloromethane solution, scan rate 60 mV s À1 , step potential 50 mV; square-wave frequency 1 Hz; and square-wave amplitude 10 mV.  indenouorene derivatives. In SQW, compound CHI1 displayed two oxidation peaks at 0.5 and 1.1 V and two reduction peaks, E red , at À1.1 and À1.2 V (vs. Ag/AgNO 3 ) using the Fc/Fc + couple as the internal standard. The onset potentials of the rst oxidation and reduction peaks were 0.35 and À 1 V respectively. The HOMO and LUMO levels were estimated from the onset potentials and converted to the vacuum scale according to the formula of HOMO ¼ À(E ox-onset + 4.8) eV, LUMO ¼ À(E red-onset + 4.8) eV. 19 According to that, the HOMO and LUMO levels were found to be at À5. 15  Both materials 7 (vacuum-deposited) and CHI1 (solutionprocessed lm) exhibited a measurable hole mobility and showed moderate charge-transport behaviour. Fig. S4 in the ESI † shows the transfer and output characteristics of an OFET. A hole mobility of 2 Â 10 À5 cm 2 V À1 s À1 was extracted from I-V output characteristic for material 7. When the substrate pre-set temperatures were increased, the device performances of 7 dramatically decreased, and no eld effect was detected at T sub ¼ 90 C. The low charge carrier mobility of 7 may be due to the unfavorable orientation of the crystallites and crystallite alignments with respect to the substrate, as evidenced by a preliminarily investigation of the crystallite orientation of the lms using grazing incidence X-ray diffraction. Moreover, the poor performance of this compound might be also attributed to a discontinuous morphology, consisting of a spherical structure, possibly hindering the charge transport by numerous grain boundaries, as evidenced by atomic force microscopy (AFM) observations, (Fig. S5 in ESI †). The bottom gate and top contact (BG/TC) OFET device for the thin lm of CHI1 spincoated from 0.3 wt% chloroform solution showed a hole mobility of 7.3 Â 10 À4 cm 2 V À1 s À1 (Fig. S6 and S7 in ESI †). The OFET devices of CHI1 were optimized and a slightly better mobility of 1.7 Â 10 À3 cm 2 V À1 s À1 was obtained for the dropcasted thin lm with the TG/BC conguration (Fig. 5).
The d-spacing obtained from the rst reection peak of the out-of-plane X-ray diffraction (XRD) pattern for the CHI1 thin lm deposited on the HMDS-treated SiO 2 substrate is 16.3Å (2q ¼ 5.43 ), which may be indexed as (102) based on the solved crystallographic structure of CHI1. The in-plane XRD of the CHI1 thin lm shows a reection peak at 2q ¼ 26.0 (d-spacing of 3.42Å) (Fig. S8 in ESI †), which corresponds to a d-spacing of p-p stacking distances between the indenoperylene cores in the crystal (3.39-3.41Å in the bulk single crystal). The surface morphologies of the CHI1 deposited on the HMDS-treated SiO 2 and PVP substrates using different processing conditions were investigated using AFM. As shown in Fig. 6, the surface morphology of the lm is strongly affected by the processing conditions, in particular, on the HMDS-treated SiO 2 (Fig. 6a) the lm shows a poor morphological order. On the other hand, on PVP substrates (Fig. 6b and c), the long-range order appears to be considerably improved and the lms are characterized by the presence of larger circular islands. Consequently, the device performance under the different processing conditions is mainly affected by the changes in the surface morphology, as shown by the AFM measurements.

Conclusions
In summary, we have developed an efficient method to prepare a new extended indenoacene derivative in which the two indene groups are introduced into a central perylene core. From a synthetic point of view, the base-promoted cyclodehydrogenation reaction of a 1,1 0 -binaphthyl derivative, bearing ketone groups positioned para to the reactive carbons in which the cyclisation occurs, using K 2 CO 3 and ethanolamine is an efficient and versatile method to build up the functionalized perylene core. The novel diindeno[1,2-b:2 0 ,1 0 -n]perylene CHI1 has a closed shell electronic conguration in the ground state which conrms that the closed or open shell character of indenoacene derivatives can be predicted just by looking at the difference in the number of aromatic sextets between the two mesomeric forms. The diindeno[1,2-b:2 0 ,1 0 -n]perylene has a quinoidal structure with a broad absorption from 400 nm up to 900 nm, a band gap of 1.35 eV and is packed into a 1-D  columnar stack in the crystal. The best OFET performance, with mobility up to 1.7 Â 10 À3 cm 2 V À1 s À1 , has been found in devices based on solution processed thin lms with a TG/BC conguration.