Introduction

Dithieno[3,2-b:2 ′ ,3 ′ -d]pyrrole (DTP) and its N-substituted derivatives are popular building blocks to prepare a wide array of conjugated organic polymers. 1,2 Due to the tunable material properties achieved by changing the structure of the monomeric unit, DTP-based polymers are employed in various applications. The optical and electronic properties of various polyDTPs have been investigated and applied in organic electronics, such as organic light-emitting diodes (OLEDs), 3,4 organic eld effect transistors (OFETs), [5][6][7][8][9] electrochromic devices, 6 organic photovoltaic devices 8,10-14 and organic batteries. 15 Additionally, N-alkyl substituted DTP homopolymers have been used as highly uorescent materials 16 and biosensors. 17,18 The majority of DTP monomers and their polymeric systems are based on dithienopyrroles with traditional alkyl and aryl side chains and are termed rst generation DTPs. 2 So-called second generation DTPs are N-acylated DTPs, which show more stable HOMO and LUMO energy levels than rst generation DTPs. 19 Recently, the synthesis of the rst N-functionalized DTP monomer with an ethynyl group was described. 20 The presence of a terminal triple bond allows for the pre-or postpolymerization modication of the corresponding monomer or polymer via 1,3-dipolar cycloaddition "click" reactions 21,22 or Sonogashira cross-coupling reactions. 22 This method can be prospective for an easy and efficient route to synthesize new bioconjugated DTP homopolymers containing various pendant groups attached to the conjugated polymer backbone via "click" reactions with corresponding organic azides. However, this technique would be easily applicable in practice only if the new N-alkynylated DTP monomer is a compact molecule, well soluble in organic solvents, and has a relatively simple synthetic preparation. To the best of our knowledge, the rst alkynylated DTP monomer described in literature 20 is the only known Nfunctionalized DTP with a terminal triple bond. Its preparation required two steps, beginning with a Buchwald-Hartwig cross-coupling reaction of 3,3 ′ -dibromo-2,2 ′ -bithiophene and 4-[(trimethylsilyl)ethynyl]-aniline, followed by the deprotection of the alkynyl group. In this product, the terminal triple bond was attached to the DTP ring by the phenyl group, which resulted in a bulky DTP molecule due to the additional aromatic ring in its structure.

Herein, a one-step synthesis of a new N-alkynylated DTP monomer via a Buchwald-Hartwig cross-coupling reaction 23 with pent-4-yn-1-amine and commercially available 3,3 ′dibromo-2,2 ′ -bithiophene is described. Additionally, a facile method to functionalize the new DTP monomer prior to polymerization via a copper-catalyzed azide/alkyne cycloaddition reaction is demonstrated. This methodology provides a rapid approach to fabricate different functionalized polyDTPs.

Materials and methods

Reagents and solvents

All chemicals were purchased from Alfa Aesar or TCI America and used without further purication. All solvents used for reactions were distilled under nitrogen aer drying over an appropriate drying reagent. All manipulations involving airand/or moisture-sensitive compounds were carried out with the standard Schlenk technique under nitrogen. . Melting points were determined on an EZ-Melt automated melting point apparatus. Analytical thin-layer chromatography was performed on glass plates coated with 0.25 mm 230-400 mesh silica gel containing a uorescent indicator. Column chromatography was performed using silica gel (spherical neutral, particle size 63-210 mm). Electrospray (ESI) mass spectra were obtained using an Agilent 6230 Time-of-Flight (TOF) spectrometer. Fourier transform infrared (FTIR) spectra were obtained with a Thermo Scientic Nicolet 6700 FTIR spectrometer and all spectra were measured using an attenuated total reection (ATR) attachment with a diamond head. Absorption spectra were obtained using a PerkinElmer Lambda 900 UV-vis/NIR spectrophotometer. A BASi 100A Electrochemical Analyzer and a C3 Cell Stand were used to perform cyclic voltammetry (CV) measurements. A KLA Alpha-HQ Prolometer was used to measure lm thickness.

Synthesis 5-Azidopent-1-yne (1). 5-Chloropent-1-tyne (9.3 g, 0.091 mol) and sodium azide (7.7 g, 0.118 mol) were added to dry dimethylformamide (20 mL). The obtained mixture was stirred at 55 C for 36 hours. Aer cooling, the mixture was ltered. The ltrate was diluted with cold water (100 mL) and extracted with dichloromethane. The organic solution was washed with water two times, separated, dried with Na 2 SO 4 , ltered, and evaporated under reduced pressure at 30 C. The product was a colorless oil, which contained 15% dimethylformamide and was used in the next step without additional purication. Yield 9.6 g (97%), clear oil. 1 H NMR (CDCl 3 , d, ppm): 1.78 (m, 2H, J ¼ 6.8 Hz), 1.99 (t, 1H, J ¼ 2.8 Hz), 2.30 (d.t, 2H, J ¼ 6.8 Hz, J ¼ 2.8 Hz), 3.43 (t, 2H, J ¼ 6.8 Hz).

Pent-4-yn-1-amine hydrochloride (2). 5-Azidopent-1-yne (1) (9.6 g, 0.088 mol) was dissolved in diethyl ether (80 mL). Triphenylphosphine (25.2 g, 0.096 mol) was added into the stirred solution in four portions at 15minutes intervals. Nitrogen gas was released, and the reaction was slightly exothermic. The obtained solution was stirred at room temperature for 14 hours, followed by the dropwise addition of concentrated hydrochloric acid (10 mL). The mixture was stirred an additional 3 hours and an amine hydrochloride solution layer precipitated on the bottom of the ask. A diethyl ether solution, which contained triphenylphosphine oxide and residual triphenylphosphine, was separated by decantation. The obtained aqueous solution of amine hydrochloride was washed with a fresh diethyl ether solution, separated, and cooled for 24 hours. The precipitated residual triphenylphosphine oxide was separated by ltration and the ltrate was evaporated and dried under reduced pressure to yield pent-4-yn-1-amine hydrochloride with a purity > 90%. The obtained product was used in the next step without additional purication. Yield 7.8 g (71%), pale yellow paste. 1 H NMR (D 2 O, d, ppm): 1.83 (m, 2H, J ¼ 6.9 Hz), 2.28-2.35 (m, 3H, J ¼ 6.9 Hz, J ¼ 2.8 Hz), 3.07 (t, 2H, J ¼ 6.9 Hz).

Pent-4-yn-1-amine (3). Pent-4-yn-1-amine (3) was prepared from its hydrochloride salt according to a previously reported method. 24 Pent-4-yn-1-amine hydrochloride (2) was dissolved in minimum deionized water, basied with sodium hydroxide, and extracted 3 times with diethyl ether. The organic solution was dried with Na 2 SO 4 and ltered. Ether was evaporated from the solution at 37 C. The residue, amine base, was used in the next step without additional purication. Pale yellow oil, yield 50%.

AlkyneDTP. AlkyneDTP was prepared by loading 3,3 ′dibromo-2,2 ′ -bithiophene (0.27 g, 0.836 mmol), pent-4-yn-1amine hydrochloride (2) (0.14 g, 1.17 mmol), BINAP (0.03 g, 0.048 mmol), Pd 2 (DBA) 3 (0.01 g, 0.011 mmol) and toluene (10 mL) in a cylindrical pressure vessel (48 mL) under nitrogen. Powdered sodium methoxide (0.23 g, 4.26 mmol) was added, and the obtained mixture was vigorously stirred in the closed vessel under nitrogen at 130 C for 24 hours. Aer cooling, the mixture was diluted with dichloromethane (10 mL) and ltered. The ltrate was evaporated under reduced pressure and the residue was puried by column chromatography. Solvent hexane/dichloromethane (2/1), R f ¼ 0.5. Yield 0.075 g (37%), pale yellow solid, mp ¼ 70-71 C. 1 H NMR (CDCl 3 , d, ppm): 2.09 (m, 3H, J ¼ 6.2 Hz, J ¼ 2.4 Hz), 2.19 (m, 2H, J ¼ 6.2 Hz, J ¼ 2.4 Hz), 4.37 (t, 2H, J ¼ 6.2 Hz), 7.07 (d, 2H, J ¼ 5.2 Hz), 7.14 (d, 2H, J ¼ 5.2 Hz). 13 The same reaction as previously described was also performed with pent-4-yn-1-amine base (3) (3 mol excess) and powdered sodium methoxide (3 mol excess) in boiling toluene for 40 hours. This reaction resulted in AlkyneDTP with a 48% yield.

AzNap. AzNap dye was prepared using a previously described method. 25 DTPNap. AlkyneDTP (0.03 g, 0.122 mmol) and AzNap (0.044 g, 0.122 mmol) were dissolved in tetrahydrofuran (6 mL) and the solution was degassed with nitrogen. An aqueous solution of sodium ascorbate (12 mg, 0.061 mmol, 1 mL H 2 O) was added into the stirred tetrahydrofuran solution, followed by an aqueous solution of copper(II) sulfate pentahydrate (9 mg, 0.037 mmol, 1 mL H 2 O). The obtained mixture was vigorously stirred at 60 C under nitrogen for 16 hours. Aer cooling, the mixture was extracted with dichloromethane and washed with water. The organic solution was dried with Na 2 SO 4 , ltered, and evaporated. The crude product was puried by column chromatography. Dichloromethane was used to wash out impurities, followed by dichloromethane/methanol (20/1) eluent, R f ¼ 0.5. Yield 0.06 g (81%), yellow solid m.p ¼ 79-80 C. 1 H NMR (CDCl 3 , d, ppm): 1.72 (m, 2H), 1.88 (m, 4H), 2.33 (m, 4H, J ¼ 6.9 Hz, J ¼ 6.5 Hz), 2.69 (t, 2H, J ¼ 6.5 Hz), 3.22 (t, 4H), 4.23 (t, 2H, J ¼ 6.5 Hz), 4.30 (t, 2H, J ¼ 5.8 Hz), 4.41 (t, 2H, J ¼ 6.9 Hz), 7.01 (d, 2H, J ¼ 5.5 Hz), 7.10 (d, 2H, J ¼ 5.5 Hz), 7.14 (d, 1H, J ¼ 7.9 Hz), 7.40 (s, 1H), 7.65 (t, 1H, J ¼ 7.6 Hz), 8.45 (d, 1H, J ¼ 7.9 Hz), 8.53 (d, 1H, J ¼ 7.6 Hz). 13

Electropolymerization

Cyclovoltammetry (CV) was performed with a BASi 100A Electrochemical Analyzer coupled to a C3 Cell Stand. p-AlkyneDTP was formed by adding 2 mL of a 0.01 M solution of AlkyneDTP in acetonitrile to 6 mL of 0.1 M tetrabutylammonium hexa-uorophosphate (TBAPF 6 ) solution in acetonitrile in a C3 Cell Stand. The cell was purged with nitrogen for 20 minutes, followed by the insertion of a 3-electrode conguration with a silver/silver chloride (Ag/AgCl) reference, platinum (Pt) counter, and either a templated indium tin oxide (ITO) or Pt button working electrode. To electropolymerize the monomer into a lm, the electrodes were cycled over 50 times at a scan rate of 100 mV s -1 from -0.5 V to +0.9 V (vs. Ag/AgCl). To ensure the lms were fully polymerized, the lms were oxidized in pure electrolyte at +1 V for 120 seconds. AlkyneDTP resulted in p-AlkyneDTP lms that were blue colored when in the oxidized form (+0.9 V) and yellow colored when in the reduced form (-0.5 V). The p-AlkyneDTP lm thickness was measured to be 255.5 nm.

p-DTPNap was formed by adding 1 mL of a 0.01 M solution of DTPNap in dichloromethane to 6 mL of 0.1 M TBAPF 6 solution in dichloromethane in a C3 Cell Stand. The cell was purged with nitrogen for 20 minutes, followed by the insertion of a 3-electrode conguration with a Ag/AgCl reference, Pt counter, and a templated ITO working electrode. To electropolymerize the monomer into a lm, the electrodes were cycled over 50 times at a scan rate of 100 mV s -1 from -0.5 V to +0.9 V (vs. Ag/AgCl). To ensure the lms were fully polymerized, the lms were oxidized in pure electrolyte at +1 V for 120 seconds. DTPNap resulted in p-DTPNap lms that were blue colored when in the oxidized form (+0.9 V) and red colored when in the reduced form (-0.5 V). The p-AlkyneDTP lm thickness was measured to be 528.3 nm. Data presented in the IUPAC redox voltage and current convention (positive potential to the right of the graph; positive/oxidizing current at the top of the graph).

Results and discussion

Synthesis

The unfunctionalized, parent dithieno[3,2-b:2 ′ ,3 ′ -d]pyrrole (DTP) molecule was rst synthesized in 1983. 26 Nearly a decade later, N-alkylated DTPs were prepared by the alkylation of the parent DTP. 27 Shortly thereaer, an improved method of N-alkyl DTP preparation was developed using Buchwald-Hartwig amination of 3-bromothiophene. 28 The current preferred synthetic method to prepare N-alkyl DTPs (cf. Scheme 1) is based on a Pdcatalyzed Buchwald-Hartwig coupling reaction of the primary amine with 3,3 ′ -dibromo-2,2 ′ -bithiophene. 29,30 This reaction achieves the highest yields with primary alkylamines by using a tris(dibenzylideneacetone)dipalladium(0) (Pd 2 (DBA) 3 ) catalyst and a 2,2 ′ -bis(diphenylphosphino)-1,1 ′ -binaphthyl (BINAP) ligand in the presence of sodium tertbutoxide (NaOtBu). However, there is no literature regarding the preparation of alkynylated dithieno[3,2-b:2 ′ ,3 ′ -d]pyrroles using Buchwald-Hartwig amination with primary alkylamines containing terminal triple bonds. This approach does not work with primary alkylamines, such as propargylamine or its higher homologs. When the reaction is performed using a Pd 2 (DBA) 3 catalyst, BINAP ligand and a NaOtBu base, only the starting compounds are detected at the end of the reaction with no nal product. In the efforts to determine a synthetic route to an alkyne-terminated DTP monomer, pent-4-yn-1-amine hydrochloride (2), it's free base (3), and commercially available propargylamine were used as starting alkylamines for the Buchwald-Hartwig amination of 3,3 ′ -dibromo-2,2 ′ -bithiophene.

Pent-4-yn-1-amine hydrochloride (2) was synthesized starting from commercially available 5-chloropent-1-yne (cf. Scheme 2). In brief, 5-chloropent-1-yne was converted into its azide derivative 5-azidopent-1-yne (1). Compound (1) was then reduced by a Staudinger reaction to the hydrochloric salt of pent-4-yn-1-amine (2). Pent-4-yn-1-amine free base (3) was isolated from its hydrochloride salt (2) by the extraction of a saturated, basied aqueous solution of compound (2) with diethyl ether. However, it was preferable to work with hydrochloride (2) because the free base (3) is volatile and well soluble in water, which makes it difficult to separate at high yields.

Having all amines in hand, a Buchwald-Hartwig coupling amination with 3,3 ′ -dibromo-2,2 ′ -bithiophene was investigated. It is important to note that when the common base for this type of coupling reaction, NaOtBu, was used, only starting compounds were observed in the reaction media aer 24 hours in boiling toluene. NaOtBu base was substituted with NaOMe, and it was found that pent-4-yn-1-amine hydrochloride (2) or its free base (3) reacted with 3,3 ′ -dibromo-2,2 ′ -bithiophene in a reuxed toluene solution in the presence of a Pd 2 (DBA) 3 catalyst, BINAP ligand, and excess MeONa to form N-alkynylated DTP AlkyneDTP (cf. Scheme 3). The same coupling reaction with propargylamine, a lower homolog of pent-4-yn-1-amine (3), was performed in a closed ask and no product was detected by NMR analysis aer several hours at 120 C in a toluene solution. Propargylamine is less nucleophilic than its higher homologs and does not react with 3,3 ′ -dibromo-2,2 ′ -bithiophene under the reaction conditions. The greatest AlkyneDTP yield (48%) was obtained when 3 moles (excess) of the amine base (3) or 2 moles of its hydrochloride salt (2) were used. The fastest reaction occurred when using the free amine base (3) and was complete aer 40 hours in boiling toluene under a nitrogen atmosphere with 3 moles MeONa. When using the hydrochloride salt (2), the reaction required 5 moles of MeONa and 48 hours in boiling toluene under a nitrogen atmosphere and ended with lower AlkyneDTP yields (37%). The reaction time could be twice reduced by raising the temperature to 130 C and using a closed, heavy wall pressure vessel.

The amination of 3,3 ′ -dibromo-2,2 ′ -bithiophene with pent-4yn-1-amine began with the formation of a mono-aminated intermediate (4). The secondary amino group in intermediate ( 4) nally reacted with a second bromine atom and formed the corresponding dithienopyrrole AlkyneDTP. The formation of the mono-aminated intermediate ( 4) occurred relatively quickly under the reaction conditions, usually within the rst 6 hours, and could be easily tracked by NMR or TLC analyses. In the NMR spectra, the methylene group (-NH-CH 2 -) in intermediate (4) has a distinct triplet at 3.34 ppm in deuterated chloroform, while the nal AlkyneDTP product has this signal shied to 4.37 ppm. The ring closure and the formation of AlkyneDTP was a slower process and took more time than the formation of the mono-aminated intermediate (4). Usually aer 24 hours at 130 • C, the reaction with pent-4-yn-1-amine hydrochloride (2) produced a mix of the nal product AlkyneDTP and the monoaminated intermediate ( 4) with a ratio 7 : 3 correspondingly. Increasing the reaction time to fully complete the process did not improve the yield because of the formation of side products. However, intermediate ( 4) could be easily separated from AlkyneDTP by column chromatography and converted to the nal AlkyneDTP with a high yield (90%) by a repeated coupling reaction.

To investigate the pre-polymerization functionalization of AlkyneDTP via copper-catalyzed 1,3-dipolar cycloaddition, an azide-modied naphthalimide dye (AzNap) 25 was used (cf. Scheme 4). The AzNap dye has a maximum absorption at 400 nm that can be easily tracked by UV-vis analysis when attached to the DTP monomer (DTPNap) and corresponding polymer (p-DTPNap).

A cycloaddition reaction of AlkyneDTP and AzNap was performed in a tetrahydrofuran/water solution and catalyzed with aqueous solutions of copper(II) sulfate pentahydrate and sodium ascorbate to generate Cu(I) in situ. 31 This reaction did not occur at room temperature and required heating at 60 C for completion. The reaction is regioselective 21,32 and, as expected, a single regioisomer of DTPNap monomer was isolated with an 81% yield.

Electropolymerization

Monomers comprising of the dithieno[3,2-b:2,3-d]pyrrole (DTP) backbone can be electrochemically and chemically polymerized. 16,[27][28][29] The two synthesized monomers, AlkyneDTP and DTPNap, were electrochemically polymerized to form lms of p-Alky-neDTP and p-DTPNap (cf. Scheme 5), respectively, on Pt button electrodes. Fig. 1a presents the 1st and 50th cyclic voltammogram of the AlkyneDTP monomer in an acetonitrile/0.1 M TBAPF 6 electrolyte. In the 1st cycle, the irreversible peak oxidation of the monomer has an onset at 770 mV.

Two very small reduction peaks at ca. 695 mV and 277 mV (which are much more evident in the 50th cycle) on the backsweep are indicative of the reduction of the initially deposited polymer. Films of polymerized AlkyneDTP (p-AlkyneDTP) were formed by substituting the Pt button working electrode with Scheme 2 Synthesis of 5-azidopent-1-yne (1) (yield 97%), pent-4-yn-1-amine hydrochloride (2) (yield 71%), and pent-4-yn-1-amine (3) (yield 50%).

Scheme 3 Synthesis of AlkyneDTP (yield 37%, 48%) and mono-aminated intermediate ( 4).

ITO-coated glass slides or Pt strips. Electropolymerizing the monomer at +1000 mV (vs. Ag/AgCl) for 150 seconds resulted in thick adherent dark-blue lms that were insoluble in water or organic solvents. This insolubility has been previously reported with electropolymerized DTP monomers. 16 These lms were conditioned prior to running their cyclic voltammograms by repeatedly cycling them in a monomer-free solution of acetonitrile/0.1 M TBAPF 6 . Cyclic voltammograms were run from -500 mV to +900 mV (100 mV s -1 ) (cf. Fig. 1b) and indicate the reversibility of the oxidation process of the p-AlkyneDTP lms by the re-tracings of the cyclic runs. This suggests that no electrochemical degradation has taken place and the onset of the oxidation potential can be related to the ionization potential (IP). The onset potential (E 0 ) was estimated from the intersection of two tangent lines drawn at the rising oxidation current and background current to give a value of 60 mV. Referring the potential value to the standard hydrogen electrode (SHE) and in turn to the vacuum level reference, the IP (estimated through IP (eV) ¼ e(E 0 + 4.4)) for p-AlkyneDTP is 4.46 eV. 33,34 Readily oxidizable conjugated polymers are characterized by IP values under 5 eV, such as poly(pyrrole) and poly(1,3ethylenedioxythiophene), which are more stable in their poly(cationic) (doped) state than in their neutral state at ambient conditions. 35 For comparison, the electrochemical properties of poly(4-(6-hexyl)-4H-dithieno[3,2-b:2 ′ ,3 ′ -d]pyrrole) (p6DTP) have been recently presented and the IP of p6DTP is 4.4 eV, a value similar to reported energy levels in some N-substituted alkyl and alkyl ether polyDTPs. [36][37][38] Fig. 2a presents the 1st cyclic voltammogram of the DTPNap monomer in a dichloro-methane/0.1 M TBAPF 6 electrolyte and is relatively featureless in comparison to the initial cyclic voltammogram of the AlkyneDTP monomer (cf. Fig. 1a). Nonetheless, there is an irreversible oxidation peak of the monomer, which has an onset at 200 mV. Films of p-DTPNap were formed with ITO-coated glass slides or Pt strips as the working electrode. Electropolymerizing the monomer at +1000 mV (vs. Ag/ AgCl) for 150 seconds resulted in thick adherent dark-blue lms that were conditioned in monomer-free electrolyte prior to running cyclic voltammograms. Fig. 2b presents a number of the cyclic voltammograms of the p-DTPNap lms indicating the reversibility of the oxidation process when cycled from -500 mV to +900 mV. With an E 0 of 160 mV, the IP is estimated to be 4.56 eV for p-AlkyneDTP.

FTIR spectroscopy

Fourier transform infrared (FTIR) spectra of the monomers were performed and compared to that of the corresponding polymers (cf. Fig. 3). As expected, the AlkyneDTP monomer exhibits the characteristic -C^Cstretch vibration as a weak narrow peak at 2116 cm -1 and a terminal alkyne C-H bond stretch appears as a strong narrow band at 3266 cm -1 . The FTIR spectra of the electropolymerized polymer p-AlkyneDTP does not show any of the characteristic alkyne bond adsorption signals. However, the FTIR spectra of p-AlkyneDTP does show strong bands in the 3000-2850 cm -1 region, conrming the presence of aliphatic -CH 2groups. These results indicate that the terminal alkyne group in AlkyneDTP was not stable during electropolymerization. Because the synthesized polymer p-AlkyneDTP no longer contained alkyne functional groups, it was not a suitable material for post-polymerization functionalization via "click" reactions with organic azides.

FTIR spectra of the DTPNap monomer contains a few bands at 3099 cm -1 , which are stretching vibrations of the triazole ] C-H bond and aromatic C-H groups. Similar to the AlkyneDTP monomer, there are aliphatic -CH 2bands observed at 2925-2849 cm -1 . The C]O carbonyl groups in the DTPNap monomer have a strong band at 1646 cm -1 but this signal as well as other bands around 1640 cm -1 disappear aer electropolymerization, which indicates the absence of carbonyl groups in p-DTPNap polymer due to their partial or complete reduction or another electrochemical reaction during electropolymerization. Similar to the DTPNap monomer, the FTIR spectra of p-DTPNap polymer has bands ranging from 3100-2800 cm -1 that correspond to aliphatic, aromatic C-H and triazole ¼ C-H groups. These results indicate that the pre-polymerization functionalization of AlkyneDTP via a 1,3-dipolar cycloaddition reaction with an azide-modied molecule is a promising route to synthesize new DTP-based monomers and electropolymerization polymers.

UV-vis spectroscopy

The optical absorbance of monomers AlkyneDTP and DTPNap in dichloromethane are presented in Fig. 4. The monomers exhibit similar absorption peaks with maximums at 227, 298, and 310 nm, as well as a shoulder at ca. 288 nm. Additionally, DTPNap exhibits a peak with a maximum at 413 nm, which is attributed to the naphthalimide dye (AzNap) attached to the monomer via a "click" reaction. 39 Spectroelectrochemical absorption properties were obtained on the corresponding polymers p-AlkyneDTP (cf. Fig. 5a) and p-DTPNap (cf. Fig. 5b) in the solid state on ITO-coated glass slides. To measure the spectroelectrochemical properties, a 3-terminal electrochemical cell with a Pt wire counter electrode, Ag/AgCl reference electrode, and the electropolymerized lms on ITOcoated glass as working electrodes were tested in a dichloromethane/0.1 M TBAPF 6 electrolyte solution. Each lm was probed at a specied voltage (+900 mV, +500 mV, -200 mV, and -500 mV (vs. Ag/AgCl)) for 120 seconds prior to measuring the optical properties by UV-vis spectroscopy. Both polymers demonstrate typical spectra for conjugated polymers undergoing redox reactions. The reduced form of p-AlkyneDTP (-500 mV (vs. Ag/AgCl)) exhibits a maximum absorption peak at 545 nm. By increasing the potential across the p-AlkyneDTP lm up to +900 mV (vs. Ag/AgCl), maximum absorption peaks at 388 nm and 760 nm appear as the reduced peak at 545 nm diminishes. Additionally, as voltage to the working electrode increased, a featureless absorption tail appeared extending from 800 nm to beyond 1350 nm. The reduced form of p-DTPNap exhibits a maximum absorption peak at 431 nm when charged at -500 mV (vs. Ag/AgCl). This maximum peak is attributed to the naphthalimide dye (AzNap) attached to the polymer via "click" reaction. By increasing the potential across the p-DTPNap lm up to +900 mV (vs. Ag/AgCl), the maximum peak blue-shis to 409 nm and a new local maximum absorption peak appears at 737 nm. Similar to p-AlkyneDTP, a featureless absorption tail appears extending from 820 nm to beyond 1200 nm.

The electronic bandgap (DE uv ) for these chemistries could be calculated from the optical absorption band edge that is observed at the absorbance onset of the neutral form of the polymer. The onset of the absorption peak for p-AlkyneDTP and p-DTPNap is observed at 703 nm and 680 nm, respectively, giving a DE uv of 1.76 eV for p-AlkyneDTP and 1.82 eV for p-DTPNap (cf. Table 1). By coupling the DE uv obtained by UV-vis with the cyclic voltammetry derived IP (i.e., HOMO) of the electropolymerized lms, the LUMO was estimated for each polymer (cf. Table 1). The p-AlkyneDTP and p-DTPNap polymers exhibit similar HOMO/LUMO energies to that of previously reported polyDTPs. [36][37][38]

Conclusion

In summary, a new N-alkylated dithieno[3,2-b:2 ′ ,3 ′ -d]pyrrole (DTP) monomer with a terminal triple bond (AlkyneDTP) was synthesized and electropolymerized (p-AlkyneDTP). The Alky-neDTP monomer was successfully functionalized before polymerization via a 1,3-dipolar cycloaddition with an azide-modied dye (AzNap) to yield a DTPNap monomer. In addition to the electropolymerization of AlkyneDTP, the DTPNap monomer was also electropolymerized (p-DTPNap). The monomers and subsequent polymers were analyzed by Fourier transform infrared (FTIR) and UV-vis spectroscopy. It was found that the alkyne functional group in the AlkyneDTP monomer was not stable during electropolymerization and was not detected in the FTIR spectra of p-AlkyneDTP. Thus, eliminating p-AlkyneDTP's candidacy for post-polymerization functionalization via 1,3-dipolar cycloaddition. However, p-DTPNap retained its pre-polymerization functionalization throughout the electropolymerization. These results afford the possibility to prepare various N-functionalized DTP monomers and corresponding polymers using 1,3-dipolar cycloaddition reactions with organic azides. The developed method allows for the addition of different functional groups to the polymeric DTP-backbone at high yields.