Synthesis of tetraselenophenoporphyrazine and its application in transistor devices †

Phthalocyanines (tetrabenzoporphyrazines) are industrially important blue/green dyes and pigments. They have also been extensively investigated for a range of other applications such as catalysts, sensors, singlet oxygen generators for photodynamic therapy, active layer materials for eld effect transistors and as photoactive materials for dye-sensitized and bulk heterojunction solar cells. For all of these applications control of the photophysical, electrochemical and morphological properties of the phthalocyanine derivative is highly important. This has typically been achieved by varying the metal or metalloid at the centre of the phthalocyanine ring, or by varying the nature of the substituents attached to the benzenoid periphery. Another approach is to change the aromatic unit fused to the porphyrazine core, for example changing from benzo(phthalocyanine) to naphtho(napthalocyanine) results in a considerable red shi of the main absorption peak into the near infrared region and signicant changes to the redox properties. In an effort to further tune the ring properties, a wide range of other hydrocarbon aromatics such as azulene, pyrene, triphenylene and helicene as well as six membered electron decient heterocycles like pyridine and pyrazine have been fused to the porphyrazine core. Encouraged by the promising charge carrier mobility of soluble substituted phthalocyanines, we were interested in

Phthalocyanines (tetrabenzoporphyrazines) are industrially important blue/green dyes and pigments.They have also been extensively investigated for a range of other applications such as catalysts, sensors, singlet oxygen generators for photodynamic therapy, active layer materials for eld effect transistors and as photoactive materials for dye-sensitized and bulk heterojunction solar cells. 1 For all of these applications control of the photophysical, electrochemical and morphological properties of the phthalocyanine derivative is highly important. 2This has typically been achieved by varying the metal or metalloid at the centre of the phthalocyanine ring, or by varying the nature of the substituents attached to the benzenoid periphery.Another approach is to change the aromatic unit fused to the porphyrazine core, for example changing from benzo(phthalocyanine) to naphtho(napthalocyanine) results in a considerable red shi of the main absorption peak into the near infrared region and signicant changes to the redox properties.In an effort to further tune the ring properties, a wide range of other hydrocarbon aromatics such as azulene, 3 pyrene, 4 triphenylene 5 and helicene 6 as well as six membered electron decient heterocycles like pyridine 7 and pyrazine 8 have been fused to the porphyrazine core.
Encouraged by the promising charge carrier mobility of soluble substituted phthalocyanines, 9 we were interested in exploring phthalocyanine analogues for possible application in eld effect transistor devices.In order to further facilitate charge transport, we reasoned that the substitution of the benzenoid ring system with an electron rich heterocycle containing a chalcogen atom would be a promising approach.Indeed the thiophene analogue (tetrathienoporphyrazine, TPz) containing four solubilising side chains has recently been reported by Takimiya and co-workers to show promising transistor performance for lms fabricated from solution. 10We were interested to investigate analogous porphyrazines in which the thiophene was replaced with selenophene.We anticipated that the inclusion of the larger, more polarisable selenium atoms might improve intermolecular contacts, as observed in other molecular species, and therefore might result in promising charge transport. 11o the best of our knowledge, selenophene containing porphyrazines have not previously been reported.In fact there are relatively few examples of porphyrazines fused with ve membered heterocycles described. 12Although electron decient examples like thiadiazole, 13 selenodiazole 14 and tellurodiazole 15 have been reported, the only well characterised examples containing electron rich heterocycles have been based on thiophene. 10,16The attempted incorporation of furan or pyrrole has been reported to result in the formation of unstable species. 17n theory selenophene could be fused to the porphyrazine ring via either the 2,3-positions or the 3,4-positions.Here we concentrate exclusively on derivatives fused via the 2,3-positions, since in the alternative case, the structure cannot be represented by a usual bonding system and is likely to be less stable.Such systems, in which one heteroatom has an unusual tetravalent bonding within the ring, have recently been reported for thiophene containing bulky substituents at the 2,5-position, but were only isolated in very low yield. 18Fusing selenophene via the 2,3-positions potentially affords a mixture of four structural isomers, differing in the relative positioning of the heteroatoms (Fig. 1).However in all structural isomers the substituent in the 5-position (peripheral position) of the selenophene has a similar relative position with respect to other isomers, which should facilitate intermolecule packing.Therefore the required solubilising side chain was included in the peripheral position of the tetraselenophenoporphyrazine ring.
The synthetic route to tetraselenophenoporphyrazine (SePz) involves the preparation of 2,3-dicyano-5-octylselenophene, which can be readily converted to a macrocycle by reaction under Linstead conditions (Scheme 1).The route is similar to that reported by Takimiya for the thiophene derivative; 10 however the reduced aromaticity and higher reactivity of selenophene over thiophene required some careful optimisation of reaction conditions.Beginning with commercially available selenophene, the octyl side chain was introduced in the 2position by treatment with one equivalent of butyllithium, followed by reaction of the resulting anion with octyl bromide.Relatively low yields of 40% were obtained aer purication by vacuum distillation.The major impurities were the 2,5-dialkylated product and unreacted starting material.Treatment of the resulting 2-octylselenophene with NBS in THF afforded 2-bromo-5-octylselenophene in 88% yield.Usage of a slight excess of NBS was found to result in a dibrominated impurity.Although this could not be separated by chromatography, it was identied as 2,4-dibromo-5-octylselenophene by comparison of the crude NMR with a sample of 2,3-dibromo-5-octylselenophene (vide infra).As expected the second electrophilic addition occurred in the more active 4-position, ortho to the alkyl chain, indicating that direct bromination was not a feasible route to the desired 2,3-dibromo-5-octylthiophene.Instead the ability of selenophene to undergo the so-called halogen dance was exploited.Thus treatment of 2-bromo-5octylselenophene with one equivalent of freshly prepared LDA resulted in lithiation in the 3-position.Upon stirring at À78 C the anion rearranged over time, most likely via an intermolecular mechanism, to afford 3-bromo-5-octylselenophene in 91% yield aer quenching with methanol.Reaction with NBS resulted in bromination in the vacant 2-position to afford 2,3dibromo-5-octylthiophene.Treatment with CuCN in hot DMF resulted in the formation of the desired 2,3-dicyano-5-octylselenophene in 60% yield.The metal free SePz was formed in 18% yield by reaction with lithium pentoxide in reuxing pentanol followed by acidic work-up.
The resulting SePz was readily soluble in a range of organic solvents, and was puried by chromatography over alumina to afford SePz as a mixture of isomers.No separation of the individual isomers was observed by normal or reverse phase chromatography.The existence of a mixture of isomers was conrmed by 1 H and 77 Se NMR (see ESI †).Assuming no steric or electronic factors favour the formation of any particular isomer, a statistical mixture would be expected with a relative ratio of 1 : 1 : 2 : 4 for C 4h , D 2h , C 2V and C s respectively.For the aromatic protons, the higher symmetry isomers (C 4h and D 2h ) would be expected to give rise to a singlet each in the 1 H NMR, whereas the lower symmetry C s and C 2v isomers could be expected to afford up to 6 singlets.Inspection of the 1 H NMR, however, shows that the aromatic protons are split into two broad signals centered at 8.33 and 8.29 ppm respectively.The proton decoupled 77 Se NMR also showed two broadly similar environments at 558 and 555 ppm, however in this case each broad peak could be resolved into four peaks suggesting that all isomers are present.
The UV-Vis absorption spectrum of SePz in chloroform and as a spun cast thin lm is shown in Fig. 2. The spectrum shows the characteristic split Q-band of a metal free phthalocyanine, with an intense maxima at 701 nm (3 219 000 M À1 cm À1 ) and a less intense broader peak at 653 nm, along with a broad Soret absorption around 360 nm.Compared to the data reported for the thiophene analogue, 19 the incorporation of selenophene  results in a red shi of 14 nm and a signicant increase in the molar absorption coefficient of 35%.Upon lm formation, the Q-band shis bathochromically to 760 nm with a signicant broadening of the absorption bands, suggestive of intermolecular interactions in the solid state.The optical band gap in the solid state, measured by the onset of absorption, is 1.51 eV, a reduction of approximately 0.05 eV compared to the thiophene analogue.SePz demonstrated good temperature stability by TGA in dry air, with the onset of decomposition (5% wt loss) occurring at 250 C.
The ionization potential of a thin lm of SePz was measured by photoelectron spectroscopy in air (PESA) and was found to be 5.27 (AE0.05)eV.This is similar to the value reported for the thiophene analogue (TPz, 5.25 eV), 19 which suggests that the reduction in band gap for SePz is mainly the result of stabilisation of the LUMO, rather than destabilisation of the HOMO similar to selenophene containing polymers. 11These results suggest that SePz may be a promising alternative to the thiophene analogue for solar cell applications, since the smaller optical band gap may potentially enhance device photocurrent, whilst the similar ionisation potential to TPz suggests no detrimental loss of the open circuit voltage.
The electronic performance of SePz was investigated in bottom gate, bottom contact eld effect transistors.Gold (Au) was used as drain-source electrodes and SiO 2 as the gate dielectric treated with HMDS.The as-spun lms of SePz exhibited clear ptype behavior with mobilities on the order of 10 À4 cm V À1 s À1 .Annealing of the devices resulted in an improvement in hole mobility, with the best performance observed for transistors annealed at 50 C which exhibited hole mobilities around 10 À2 cm V À1 s À1 with channel current on/off ratios in excess of 10 4 (Fig. 3).Annealing at higher temperatures up to 150 C did not result in any further improvement in device performance.Comparison of Fig. 3 with the performance characteristics of other phthalocyanine-based transistors is not straightforward due to the signicant impact of device geometry as well as the non-optimized lm morphology of SePz.Despite this, however, the present results show that SePz is amongst the best performing solution processed phthalocyanines reported to date. 9,10 In conclusion we have reported the synthesis of the rst selenophene containing porphyrazine derivative, tetraselenophenoporphyrazine, as an inseparable mixture of isomers.The macrocycle exhibits a strong and sharp absorption in the visible region in solution, with a signicant broadening and red shi upon lm formation, indicative of ordering in the solid state.Field effect transistors fabricated from solution exhibit promising mobilities on the order of 10 À2 cm V À1 s À1 .This work was supported by the EPRSC (EP/I002936/1 and EP/G060738/1).We thank Scott E. Watkins (CSIRO Materials Science and Engineering, Victoria, Australia) for performing PESA measurements.

Fig. 2
Fig.2UV-Vis absorption spectra of SePz in CHCl 3 and as a spun cast film.