FOR THEIR SYNTHESIS

This invention provides the novel electron-rich heterocycles possessing unique structure and properties, which can be used as strongly fluorescent compounds and the one-stage method of their synthesis from simple substrates.

There is a requirement for new strongly fluorescent materials, due to the development of fluorometric techniques and intensification of their use in modern biomedical techniques and in diagnostics (e. g. optical imaging). Moreover the development of compounds, which display high fluorescent quantum yields is particularly desirable.

Under such circumstances, invented l,4-dihydropyrrolo[3,2-6]pyrroles, which possess superb optical properties, have the potential to be molecule of choice for above applications.

The subject mater of invention is a compound of formula (I):

wherein R ¹ , R ² and R ³ each independently stands for hydrogen or optionally substituted: alkyl, aryl, arylethynylaryl or heteroaryl, with the exception of the compound of formula (I) wherein R ¹ = R ² = R ³ = H.

The term "aryl" means, unless otherwise stated, unsubstituted benzene, naphthalene, fluorene, 9,9- dialkylfluorene, or anthracene as well as benzene ring possessing the following substituents in ortho, meta or para positions: CN, C0 ₂ Me, C0 ₂ Et, S0 ₃ H, CHO, CONH ₂ , F, CI, Br, I, N0 ₂ , OMe, OCH ₂ 0, NH ₂ , NMe ₂ , SF ₅ .

The term "heteroaryl" refers to five-membered or six-membered aromatic ring that contain at least one heteroatom selected from N, O, S and Se. Examples of heteroaryl groups include pyridine, furan, pyrrole, thiophene, oxazole, imidazole, thiazole, pyrimidine.

The term "arylethynylaryl" refers to two benzene rings linked by carbon-carbon triple bond, possessing such substituents as: N0 ₂ , CN, OMe, S0 ₂ Me, S0 ₃ H, F, CI, Br, I, CHO, COOH, CONH ₂ , SF ₅ .

The term "alkyl" by itself or as part of another substituent, means, unless otherwise stated, a straight or branched chain with general formula: C _n H _2n+ i e.g. methyl, ethyl, «-propyl, isopropyl, «-butyl and tert- butyl.

Preferably, R ³ is hydrogen atom. Also preferably, R ¹ and R ² , each independently, are aryl or heteroaryl substituents. Especially preferably, R ¹ and R ² are derivatives of benzene, optionally substituted in ortho, meta, para position with a member selected from: N0 ₂ , CN, OMe, S0 ₂ Me, S0 ₃ H, F, CI, Br, I, CHO, COOH, CONH ₂ .

Preferably, compounds according to the invention have general formula (II):

(II)

wherein Ar ¹ and Ar ² each independently stands for optionally substituted: aryl or heteroaryl, as defined above.

Preferably, compounds according to the invention have general formula III or IV:

HI IV wherein Ar ¹ , Ar ² and Ar ³ each independently stands for optionally substituted: aryl or heteroaryl, as defined above.

Preferably, compounds according to the invention have general formula V:

V wherein Ar ² and Ar ⁴ each independently stands for optionally substituted: aryl or heteroaryl, as defined above.

Preferably, the compound according to the invention is selected from the group consisting of: compounds 1-15, compounds 16-26 (i.e. compound possessing general formula II), compounds 27- 34 (i.e. compounds possessing general formulas III or IV) and compounds 35-39 (i.e. compound possessing general formula V), which have been enumerated and depicted below:

2,5-diphenyl-l,4-bis(4-methylphenyl)-l,4-dihydropyrrolo[3 ,2-6]pyrrole (1), l,2,4,5-tetra(4-methylphenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole (2),

2,5 -di(naphthalen- 1 -yl)- 1 ,4-bis(4-methylphenyl)- 1 ,4-dihydropyrrolo [3,2-6]pyrrole (3),

2,5-di(anthracen-9-yl)-l,4-bis(4-octylphenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole (4),

2,5-bis(4-cyanophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydr opyrrolo[3,2-6]pyrrole (5),

2,5-bis(3-cyanophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydr opyrrolo[3,2-6]pyrrole (6),

2,5-bis(2-cyanophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydr opyrrolo[3,2-6]pyrrole (7),

1.4- bis(4-bromophenyl)-2,5-bis(4-methylphenyl)-l,4-dihydropyrrol o[3,2-6]pyrrole (8),

2.5- bis(4-methoxyphenyl)-l,4-bis(4-methylphenyl)-l,4-dihydropyrr olo[3,2-6]pyrrole (9),

2,5-bis(benzo[( ][l,3]dioxol-5-yl)- l,4-bis(4-methylphenyl)-l,4-dihydropyrrolo[3,2-6]pyrrole (10),

1.4- bis(4-chlorophenyl)-2,5-bis(4-cyanophenyl)-l,4-dihydropyrrol o[3,2-6]pyrrole (11),

2.5- bis(4-fluorophenyl)-l,4-bis(4-methoxyphenyl)-l,4-dihydropyrr olo[3,2-6]pyrrole (12),

1.4- bis(4-nitrophenyl)-2,5-bis(4-methylphenyl)-l,4-dihydropyrrol o[3,2-6]pyrrole (13),

2.5- bis(3-nitrophenyl)-l,4-bis(4-octylphenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole (14),

2,5-di(pyridin-3-yl)-l,4-bis(4-methylphenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole (15),

1.4- bis(4-methylphenyl)-2,5-bis(4-((trime^

(16),

2.5- bis(2-bromophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydropyrrol o[3,2-6]pyrrole (17),

2,5-bis(2-methoxyphenyl)-l,4-bis(4-methylphenyl)-l,4-dihy dropyrrolo[3,2-6]pyrrole (18),

2,5-bis(2-(allyloxy)phenyl)-l,4-bis(4-methylphenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole (19), l,4-bis(4-methylphenyl)-2,5-bis(4-(pentafluoro-

(20),

l,2,4,5-tetrakis(4-(pentafluoro-A ⁶ -sulfanyl)phenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole (21),

1.4- bis(4-bromophenyl)-2,5-bis(4-cyanophenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole (22),

2.5- bis(4-bromo-2-nitrophenyl)- 1 ,443is(44iexylphenyl)- 1 ,4-dihydropyrrolo[3,2-fc]pyrrole (23), 2,5-bis(benzo[6]thiophen-2-yl)- bis(4-methylphenyl)-l,4-dihydropyrrolo[3,2-6]pyrrole (24), 2,5-di(benzofuran-2-yl)-l,4-bis(4-methylphenyl)-l,4-dihydrop yrrolo[3,2-6]pyrrole (25),

1.4- bis(4-methylphenyl)-2,5-bis(thiazol-2-yl)- l,4-dihydropyrrolo[3,2-6]pyrrole (26),

2.5- bis(4-cyanophenyl)-3-(9,9-dioctyl-9H-fluoren-3-yl)-l,4-bis(4 -methylphenyl)-dihydropyrrolo[3,2- 6]pyrrole(27),

2,5-bis(4-cyanophenyl)-l,4-bis(4-methylphenyl)-3-(4-nto

2,5-bis(4-cyanophenyl)-l,4-bis(4-methylphenyl)-3,6-bis-(4-ni trophenyl)-dihydropyrrolo[3,^ 6]pyrrole(29),

2,5-bis(4-cyanophenyl)-l,4-bis(4-methylphenyl)-3,6-bis(4-(pe ntafluoro-A ⁶ -sulfanyl)phenyl)- l,4- dihydropyrrolo[3,2-6]pyrrole(30),

2,5-bis(4-cyanophenyl)-l,4-bis(4-methylphenyl)-3-(pyridin-3- yl)- l,4-dihydropyrrolo[3,2- 6]pyrrole(31), 2,5-bis(4-cyanophenyl)-l,4-bis(4-memylphenyl)-3,6-di(pyridin -3-yl)- l,4-dihydropyrrolo[3,^ 6]pyrrole (32),

2,3,5 ris(4-cyanophenyl)- l,4-bis(4-methylphenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole(33),

2,5-bis(4-cyanophenyl)-3-(4-methoxyphenyl)-l,4-bis(4-methylp henyl)- l,4-dihydropyrrolo[3,^

6]pyrrole(34),

2,5-bis(4-(4-cyanoemynylphenyl)phenyl)-l,4-bis(4-m

(35),

2,5- bis(4-(4-pentafluoromiophenyl)ethynylphenyl)- l,4-bis(4-methylphenyl)-l,4-dihydro^

6]pyrole (36),

2,5- bis(4-(4-trifluoromethyl)ethynylphe^^

6]pyrrole (37),

2,5- bis(4-(3,5-di(trifluoromethyl)ethyn^

6]pyrrole (38),

2,5- bis(4-(methoxy)ethynylphenyl)- l,4-bis(4-methylphenyl)- l,4-dihydropyrrolo[3,2-6]pyrrole (39).

The next subject of the invention is the method of synthesis compound of formula (II):

(II)

wherein Ar ¹ and Ar ² are substituents selected from aryl or heteroaryl. General procedure involves reaction of butane-2,3-dione with arylaldehyde with formula Ar^HO and arylamine with formula Ar ² NH ₂ in acidic conditions. Further isolation leads to compound II.

Preferably, the reaction is performed in acetic acid, particularly in glacial acetic acid. Further, the reaction may be carried out at temperature above 50 °C in particular around 100 °C. Compound with a formula II precipitates from reaction mixture and further filtration affords pure product.

Preferably, the reaction is performed in the presence of Bronsted acid as catalyst, especially Bronsted acid with pK _a < 2, in particular arylsulfonic acid, especially such as / toluenosulfonic acid or benzenesulfonic acid. Further, the reaction may be carried out at room temperature or under heating, e.g. at a temperature of 50°C- 1 10°C. Compound with a formula (II) precipitates from reaction mixture and further filtration affords pure product.

This synthetic methodology has significant advantage over previous one. The yields of products are significantly ( 1.3-3) higher than without catalyst. This is especially pronounced if Ar ¹ possess ortho substituents (entries 4, 5, 6).

[a] cat.- pTsOH, benzenesulfonic acid [b] isolated yield without catalyst,

[c] isolated yield after addition of catalyst to the reaction mixture.

The most characteristic feature of compounds synthesized according to the present invention is a strong absorption of UV and visible-light in range violet to greenish-blue. Their color oscillates between colorless, through yellow and orange to red (Fig. 1). Compounds of the invention, which possess electron-donating groups and halogens, are colorless. Moreover, all of synthesized compounds are fluorescent and they emit blue or violet light both in a solution and (what is very rare) in solid state. Few exceptions from this rule are compounds possessing N0 ₂ group, which quenches fluorescence. However they possess very intense orange-red color in solid state, which makes them dyes. Moreover N0 ₂ group decrease solubility of a dye in water or in organic solvents. Consequently they can be used as pigments, which is preferable from the point of view of industrial uses. Compounds synthesized according to the present invention possess strong absorption of light in a range 280-520 nm (molar absorption coefficient is 10000 - 71000 units). It means that in a various practical applications, less substance can be used with the same final effect. However the most important is fact that fluorescence quantum yields are very high (usually above 50%). Detailed optical parameters (i.e. absorption maxima, emission maxima, molar absorption coefficient and fluorescence quantum yield) are shown in Table 1. All, the most characteristic examples are presented there. Compounds synthesized according to the present invention are characterized by their quadrupolic structure what may influence on high value of two photon cross section, thus may be applied in two- photon excited fluorescence (TPEF) microscopy.

Compounds of the invention may be obtained in a multicomponent reaction from simple substrates i.e. aldehydes, amines and diacetyl. Acetic acid, which serves as a solvent as well as precipitation of a product from reaction mixture, make this synthetic process is operationally simple, fast, economic and ecologic.

The following examples exemplify the invention without limiting it.

Example 1. General synthetic method (compound of formula II)

A variant carried out without catalyst:

1 -15

In a 25 ml round-bottom flask equipped with a reflux condenser and magnetic stirrer were placed 5 mL glacial acetic acid, butane-2,3-dione ( 1 mmol), arylamine (2 mmol), aldehyde (2 mmol). The resulting mixture was stirred at 100°C for 3h. Then reaction mixture was cooled to room temperature. Resulting precipitate was then filtered off and washed with cold glacial acetic acid. Recrystallization from AcOEt followed by drying under vacuum afforded pure product.

A variant carried out in presence of catalyst:

1-15

In a 25 ml round-bottom flask equipped with a reflux condenser and magnetic stirrer were placed 5 mL glacial acetic acid, butane-2,3-dione (1 mmol), arylamine (2 mmol), aldehyde (2 mmol) and p-toluenesulfonic acid (0.2 mmol). The resulting mixture was stirred at 100 °C for 3h. Then reaction mixture was cooled to room temperature. Resulting precipitate was then filtered off and washed with cold glacial acetic acid. Recrystallization from AcOEt followed by drying under vacuum afforded pure product.

In examples 2-16 the syntheses of compounds 1- 15 have been described.

Example 2. 2,5-diphenyl-l,4-bis(4-methylphenyl)-l,4-dihydropyrrolo[3,2- Z>]pyrrole (1)

Beige solid. Yield 145 mg (33%). R _/= 0.86 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 239 - 244 °C (CH ₃ C0 ₂ H). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.22 (ΑΑ'ΧΧ', 4H), 7.21 (ΑΑ'ΧΧ' , 4H), 7.19 - 7.13 (m, 10H), 6.38 (s, 2H), 2.36 (s, 6H). ¹³ C NMR (125 MHz, CDC1 ₃ ) (3137.5, 135.7, 135.3, 133.8, 131.6, 129.6, 128.2, 128.1, 126.0, 125.0, 94.5, 21.0. HRMS (EI) calcd for C ₃₂ H ₂₆ N ₂ : 438.2096 [M ⁺ ], found: 438.2100. Anal, calcd for C ₃₂ H ₂₆ N ₂ : C, 87.64; H, 5.98; N, 6.39; found: C, 87.79; H, 5.97; N, 6.40. A _abs (CH ₃ C1, ε x 10 ³ ) 348 (33) nm.

Example 3. l,2,4,5-tetra(4-methylphenyl)-l,4-dihydropyrrolo[3,2-Z>]p yrrole (2)

White solid. Yield 158 mg (34%). ^ R _f = 0.71 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 261 - 262 °C (CH ₃ C0 ₂ H). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.17 (ΑΑ'ΧΧ', 4H), 7.15 (ΑΑ'ΧΧ', 4H), 7.11 (ΑΑ'ΧΧ', 4Η), 7.02(ΑΑ'ΧΧ' , 4Η), 6.33 (s, 2Η), 2.36 (s, 6Η), 2.30 (s, 6H). ¹³ C NMR ( 125 MHz, CDC1 ₃ ) δ 137.7, 135.7, 135.6, 135.1, 131.3, 131.0, 129.6, 128.8, 128.0, 125.0, 94.1, 21.1, 21.0. HRMS (EI) calcd for C ₃₄ H ₃₀ N ₂ : 466.2409 [M ⁺ ], found: 466.2406. Anal, calcd for C ₃₄ H ₃₀ N ₂ : C, 87.52; H, 6.48; N, 6.00; found: C, 87.47; H, 6.43; N, 5.94. A _abs (CH ₂ Cl ₂ ,e x 10 ³ ) 348 (37) nm. Example 4.2,5-di(naphthalen-l-yl)-l,4-bis(4-methylphenyl)-l,4-dihydr opyrrolo[3,2-Z>]pyrrole (3)

Yellow solid. Yield 270 mg (50%). ^M R _/= 0.61 (Si0 ₂ , AcOEt/hexanes, 1:2). Mp 249 - 252 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 8.26 (d, / = 7.9 Hz, 2H), 7.84 (d, / = 7.6 Hz, 2 H), 7.77 (d, / = 7.9 Hz, 2H), 7.46-7.32 (m, 8H), 7.10 (ΑΑ'ΧΧ', 4H), 6.95 (ΑΑ'ΧΧ', 4H), 6.55 (s, 2H), 2.23 (s, 6H). ¹³ C NMR (500 MHz, CDC1 ₃ ) (3137.4, 134.6, 133.8, 132.9, 132.5, 131.7, 130.4, 129.4, 129.0, 128.0, 127.4, 126.6, 126.0, 125.7, 125.1, 123.9, 97.0, 20.9. HRMS (EI) calcd for C ₄₀ H ₃₀ N ₂ : 538.2409 [M ⁺ ], found: 538.2419. Anal, calcd for C ₄₀ H ₃₀ N ₂ : C, 89.19; H, 5.61; N, 5.20; found: C, 89.14; H, 5.70; N, 5.17. A _abs (toluene, ε x 10 ³ ) 377 (14) ran.

Example 5. 2,5-di(anthracen-9-yl)-l,4-bis(4-octylphenyl)-l,4-dihydropyr rolo[3,2-Z>]pyrrole (4)

Orange solid. Yield 93 mg ( 11%). ^M R _f = 0.74 (Si0 ₂ , AcOEt/hexanes, 1:9). Mp 223 - 224 °C . ¾ NMR (500 MHz, CDC1 ₃ ) δ 8.46 (s, 2H), 8.22 - 8.14 (m, 4H), 8.03 - 7.94 (m, 4H), 7.47 - 7.34 (m, 8H), 7.01 (ΑΑ'ΧΧ' , 4H), 6.72 (ΑΑ'ΧΧ', 4H), 6.61 (s, 2H), 2.37 - 2.24 (m, 4H), 1.32 - 1.39 (m, 4H), 1.20 - 1.27 (m, 4H), 1.14 - 1.19 (m, 12H), 1.05 - 1.13 (m, 4H), 0.83 (t, J = 7.1 Hz, 6H). ¹³ C NMR (500 MHz, CDCI ₃ ) (3 139.3, 137.6, 132.3, 131.3, 130.1, 130.0, 128.9, 128.5, 128.2, 127.4, 127.2, 125.7, 125.1, 122.9, 98.3, 35.1, 31.8, 31.0, 29.3, 29.2, 29.1, 22.6, 14.1. HRMS (EI) calcd for (C ₆₂ H ₆₂ N ₂ ), 834.4913 [M ⁺ ]; found, 834.4900. Anal, calcd for C ₆₂ H ₆₂ N ₂ : C, 89.16; H, 7.48; N, 3.35. Found: C, 89.15; H, 7.42; N, 3.29. A _abs (toluene ε x 10 ³ ) 387 (35) nm.

Example 6. 2,5-bis(4-cyanophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydropy rrolo[3,2-Z>] pyrrole (5)

Yellow-green solid. Yield 180 mg (37%). ^[c] R _/= 0.65 (Si0 ₂ , CH ₂ C1 ₂ ). Mp 319-321 °C (AcOEt). ¾ NMR (600 MHz, CDC1 ₃ ) δ 7.47 (ΑΑ'ΧΧ', 4H), 7.27 (ΑΑ'ΧΧ', 4H), 7.21 (ΑΑ'ΧΧ', 4Η), 7.14 (ΑΑ'ΧΧ' , 4Η), 6.45 (s, 2Η), 2.40 (s, 6H); ¹³ C NMR (150 MHz, CDC1 ₃ ) δ 137.7, 136.7, 136.5, 135.0, 133.4, 131.9, 130.1, 127.8, 125.2, 119.1, 109.0, 95.8, 21.1. HRMS (FD-TOF) calcd for C ₃₄ H ₂₄ N ₄ : 488.2001 [M ⁺ ], found: 488.2014. Anal, calcd for C ₃₄ H ₂₄ N ₄ : C, 83.58; H, 4.95; N, 11.47; found: C, 83.53; H, 4.97; N, 11.33. A _abs (CH ₂ C1 ₂ , ε x 10 ³ ) 405 (54) nm.

Example 7. 2,5-bis(3-cyanophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydropy rrolo[3,2-Z>] pyrrole (6)

Yellow solid. Yield 166 mg (34%). ^[c] R _/= 0.52 (Si0 ₂ , AcOEt/hexanes, 1:2). Mp 314 - 316 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.51 (t, / = 1.5 Hz, 2H), 7.42 (dd, / = 7.6, 1.4 Hz, 2H), 7.40 - 7.36 (m, 2H), 7.20 (ΑΑ'ΧΧ' , 4H), 7.13 (ΑΑ'ΧΧ', 4H), 6.41 (s, 2H), 2.40 (s, 6H). ¹³ C NMR ( 125 MHz, CDC1 ₃ ) δ 136.6, 136.4, 134.7, 134.0, 132.5, 132.0, 131.0, 130.1, 129.4, 128.9, 125.1, 118.7, 112.4, 95.3, 21.1. HRMS (ESI) calcd for C ₃₄ H ₂₄ N ₄ : 488.2001 [M ⁺ ], found: 488.1999. Anal, calcd for C ₃₄ H ₂₄ N ₄ : C, 83.58; H, 4.95; N, 11.47; found: C, 83.73; H, 4.86; N, 11.45. A _abs (CH ₂ Cl ₂ ,e x 10 ³ ) 368 (33) nm.

Example 8. 2,5-bis(2-cyanophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydropy rrolo[3,2-Z>] pyrrole (7)

Yellow solid. Yield 23 mg (5%). ^M R _/= 0.37 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 344-345 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.66 (dd, / = 7.8, 1.1 Hz, 2H), 7.37 (dd, / = 7.7, 1.3 Hz, 2H), 7.30 - 7.27 (m, 2H), 7.16 - 7.09 (m, 10H), 6.66 (s, 2H), 2.35 (s, 6H). ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 137.1, 136.6, 135.7, 133.7, 132.0, 131.9, 131.8, 131.1, 129.9, 126.7, 124.9, 118.8, 111.4, 97.2, 21.0. HRMS (EI) calcd for C ₃₄ H ₂₄ N ₄ : 488.1988 [M ⁺ ], found: 488.1989. Anal, calcd for C ₃₄ H ₂₄ N ₄ : C, 83.58; H, 4.95; N, 11.47; found: C, 83.50; H, 4.91 ; N, 11.54. A _abs (toluene, ε x 10 ³ ) 388 (10) nm. Example 9. l,4-bis(4-bromophenyl)-2,5-bis(4-methylphenyl)-l,4-dihydropy rrolo[3,2-Z>]pyrrole

(8)

White solid. Yield 133 mg (22%). ^[c] R _/= 0.71 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 297 - 298 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.46 (ΑΑ'ΧΧ', 4H), 7.14 (ΑΑ'ΧΧ' , 4H), 7.09 (ΑΑ'ΧΧ', 4Η), 7.05 (ΑΑ'ΧΧ' , 4Η), 6.34 (s, 2Η), 2.32 (s, 6Η). ¹³ C NMR ( 125 MHz, CDC1 ₃ ) δ 139.1, 136.3, 135.8, 132.2, 131.0, 130.3, 129.1, 128.2, 126.6, 118.9, 94.9, 21.2. HRMS (EI) calcd for C ₃₂ H ₂₄ Br ₂ N ₂ : 594.0306 [M ⁺ ], found: 594.0322. Anal, calcd for C ₃₂ H ₂₄ Br ₂ N ₂ : C, 64.45; H, 4.06; Br, 26.8; N, 4.7; found: C, 64.44; H, 4.15; Br, 26.75, N, 4.60. A _abs (CHC1 ₃ , ε x 10 ³ ) 304 (35), 348 (33) nm.

Example 10. 2,5-bis(4-methoxyphenyl)-l ,4-bis(4-methylphenyl)-l ,4-dihydropyrrolo [3,2- b] pyrrole (9)

White solid. Yield 77 mg (15%). R _/= 0.60 (Si0 ₂ , AcOEt/hexanes, 1:2). Mp 241 - 242 °C (CH ₃ C0 ₂ H). ¾ NMR (500 MHz, C ₆ D ₆ ) δ 7.31 (ΑΑ'ΧΧ', 4H), 7.28 (ΑΑ'ΧΧ', 4H), 6.89 (ΑΑ'ΧΧ' , 4Η), 6.69 (ΑΑ'ΧΧ', 4Η), 6.54 (s, 2Η), 3.25 (s, 6Η), 2.04 (s, 6H). ¹³ C NMR (125 MHz, C ₆ D ₆ ) δ 158.7, 138.6, 135.6, 135.0, 132.1, 130.0, 129.8, 125.6, 114.1, 94.8, 54.7, 20.8.HRMS (FD)calcd for C ₃₄ H ₃₀ N ₂ O ₂ : 498.2307 [M ⁺ ], found: 498.2307. Anal, calcd for C ₃₄ H ₃₀ N ₂ O ₂ : C, 81.90; H, 6.06; N, 5.62; found: C, 81.73; H, 5.87; N, 5.51. A _abs (toluene, ε x 10 ³ ) 300 (27), 348 (36) nm.

Example 11. 2,5-bis(benzo[i/[ [l,3]dioxol-5-yl)-l,4-bis(4-methylphenyl)-l,4-dihydropyrrolo [3,2- bjpyrrole (10)

Colorless solid. Yield 137 mg (13%). R _/= 0.66 (Si0 ₂ , AcOEt/hexanes, 1:2). Mp 236 - 237 °C (AcOEt). ¾ NMR (500 MHz, C ₆ D ₆ ) δ 7.23 (ΑΑ'ΧΧ', 4H), 6.92 (d, / = 1.7 Hz, 2H), 6.87 (ΑΑ'ΧΧ' , 4H), 6.81 (dd, / = 8.1, 1.7 Hz, 2H), 6.56 (d, / = 8.1 Hz, 2H), 6.43 (s, 2H), 5.23 (s, 4H), 2.02 (s, 6H). ¹³ C NMR (125 MHz, C ₆ D ₆ ) δ 148.0, 146.6, 138.4, 135.7, 135.2, 132.1, 130.0, 128.9, 125.5, 122.3, 109.2, 108.5, 100.9, 95.1, 20.8. HRMS (EI) calcd for C ₃₄ H ₂₆ N ₂ 0 ₄ : 526.1879 [M ⁺ ], found: 526.1882. Anal, calcd forC ₃₄ H ₂₆ N ₂ 0 ₄ : C, 77.55; H, 4.98; N, 5.32; found: C, 77.56; H, 4.94; N, 5.35. A _abs (toluene, ε x 10 ^"3 ) 304 (23), 354 (37) nm.

Example 12. 1 ,4-bis(4-chlorophenyl)-2,5-bis(4-cyanophenyl)-l ,4-dihydropyrrolo [3,2-Z>] pyrrole (11)

Yellow solid. Yield 33 mg (6%). ^M R _f = 0.65 (Si0 ₂ , AcOEt/hexanes, 1:2). Mp 324-325 °C (CH ₃ C0 ₂ H). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.52 (ΑΑ'ΧΧ', 4H), 7.40 (ΑΑ'ΧΧ' , 4H), 7.28 (ΑΑ'ΧΧ', 4Η), 7.20 (ΑΑ'ΧΧ' , 4Η), 6.47 (s, 2Η). ¹³ C NMR ( 125 MHz, CDC1 ₃ ) δ 137.7, 137.1, 135.2, 133.1, 132.4, 132.2, 129.8, 128.0, 126.4, 118.8, 109.7, 96.5. HRMS (EI) calcd for C ₃₂ H ₁₈ C1 ₂ N ₄ : 528.0905 [M ⁺ ], found: 528.0905. Anal, calcd for C ₃₂ H ₁₈ C1 ₂ N ₄ : C, 72.60; H, 3.43;C1, 13.39; N, 10.58; found: C, 72.50; H, 3.45; CI, 13.37; N, 10.52. A _abs (CHC1 ₃ , ε x 10 ³ ) 399 (49) nm.

Example 13. 2,5-bis(4-fluorophenyl)-l ,4-bis(4-methoxyphenyl)-l ,4-dihydropyrrolo [3,2-Z>] pyrrole (12)

Colorless solid. Yield 51 mg (7%). ^M R _/= 0.86 (Si0 ₂ , AcOEt/hexanes, 1:2). Mp 261 - 263 °C (CH ₃ C0 ₂ H). ¾ NMR (500 MHz, C ₆ D ₆ ) δ 7.15 (ΑΑ'ΧΧ', 4H), 7.13 (ΑΑ'ΧΧ', 4H), 6.71 (ΑΑ'ΧΧ' , 4Η), 6.66 (ΑΑ'ΧΧ', 4Η), 6.39 (s, 2Η), 3.23 (s, 6Η). ¹³ C NMR (125 MHz, C ₆ D ₆ ) δ 162.8, 160.9, 158.2, 135.1, 133.6, 132.6, 130.7, 130.6, 130.1, 130.0, 127.0, 115.5, 115.3, 114.7, 94.6, 54.9. HRMS (EI) calcd for C ₃₂ H ₂₄ F ₂ N ₂ 0 ₂ : 506.1806 [M ⁺ ], found: 506.1815. Anal, calcd for C ₃₂ H ₂₄ F ₂ N ₂ 0 ₂ : C, 75.88; H, 4.78; F, 7.50; N, 5.53; found: C, 76.04; H, 4.79; F, 7.53; N, 5.48. A _abs (toluene, ε x 10 ³ ) 345 (34) nm. Example 14. 1 ,4-bis(4-nitrophenyl)-2,5-bis(4-methylphenyl)-l ,4-dihydropyrrolo [3,2-Z>] pyrrole

(13)

Red solid. Yield 55 mg (11%). ^M R _/= 0.50 (Si0 ₂ , AcOEt/hexanes, 1:2). Mp 317 - 319 °C (CH ₃ C0 ₂ H). ¾ NMR (500 MHz, DMSO) δ 8.28 (ΑΑ'ΧΧ', 4H), 7.50 (ΑΑ'ΧΧ', 4H), 7.13 - 7.17 (m, 8H), 6.69 (s, 2H), 2.30 (s, 6H). HRMS (EI) calcd for C ₃₂ H ₂₄ N ₄ 0 ₄ : 528.1790 [M ⁺ ], found: 528.1798. Anal, calcd for C ₃₂ H ₂₄ N ₄ 0 ₄ : C, 72.72; H, 4.58; N, 10.60; found: C, 72.63; H, 4.44; N, 10.57. A _abs (CHC1 ₃ , ε x 10 ³ ) 360 (41) nm.

Example 15. 2,5-bis(3-nitrophenyl)-l,4-bis(4-octylphenyl)-l,4-dihydropyr rolo[3,2-Z>]pyrrole (14)

The resulting orange solid was filtered off and washed with cooled glacial acetic acid. Column chromatography (AcOEt/hexanes, 1:2) and crystallization from AcOEt gave pure product (84 mg, 12%) ^M . R _{/ =} 0.77 (Si0 ₂ , AcOEt/hexanes, 1:9). Mp 193 - 194 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 8.14 (m, 2H), 7.97 (ddd, / = 8.1, 2.3, 1.0 Hz, 2H), 7.42 (ddd, / = 7.8, 1.7, 1.1 Hz, 2H), 7.33 (m,2H), 7.22 (ΑΑ'ΧΧ' , 4H), 7.18 (ΑΑ'ΧΧ' , 4H), 6.50 (s, 2H), 2.69 - 2.60 (m, 4H), 1.70 - 1.59 (m, 4H), 1.40 - 1.20 (m, 20H), 0.89 (t, / = 7.0 Hz, 6H). ¹ C NMR (125 MHz, CDC1 ₃ ) S 148.3, 141.6, 136.7, 135.1, 134.1, 133.4, 132.7, 129.5, 128.9, 125.3, 122.2, 120.6, 95.4, 35.5, 31.9, 31.3, 29.4, 29.3, 29.2, 22.7, 14.1. HRMS (EI) calcd for ^Η ₅₂ Ν ₄ 0 ₄ : 724.3989 [M ⁺ ], found: 724.3987. Anal, calcd for ^Η ₅₂ Ν ₄ 0 ₄ : C, 76.21 ; H, 7.23; N, 7.73; found: C, 76.21 ; H, 7.12; N, 7.74. A _abs (CHC1 ₃ , ε x 10 ³ ) 361 (39) nm.

Example 16. 2,5-di(pyridin-3-yl)-l,4-bis(4-methylphenyl)-l,4-dihydropyrr olo[3,2-Z>]pyrrole (15)

Product didn't precipitate from reaction mixture. Acid was evaporated and residue was dissolved in Na ₂ C0 _3(aq) and extracted three times with dichloromethane (30 ml). Organic layers were combined, dried over Na ₂ S0 ₄ and concentrated under reduced pressure. The residual oil was purified by flash column chromatography (Si0 ₂ , CH ₂ Cl ₂ /MeOH, 95:5). Beige solid. Yield 10 mg (1 ). ^M R _{/ =} 0.41 (Si0 ₂ , CH ₂ Cl ₂ /MeOH, 95:5). Mp. 216 °C (AcOEt, decomp.) ¾ NMR (500 MHz, CDC1 ₃ ) δ 8.55 (d, /= 1.6 Hz, 2H), 8.37 - 8.40 (m, 2H), 7.45 - 7.48 (m, 2H), 7.14 - 7.23 (m, 10H), 6.43 (s, 2H), 2.39 (s, 6H). ¹³ C NMR ( 125 MHz, CDC1 ₃ ) δ 147.8, 146.0, 136.6, 136.5, 135.5, 132.7, 132.5, 130.1, 130.0, 125.3, 123.2, 95.1, 21.0. LRMS (API) calcd for C ₃₀ H ₂₄ N ₄ : 441.2 [M+H ⁺ ], found: 441.5. A _abs (CHC1 ₃ , ε x 10 ³ ) 361 (47) nm.

In examples 17-27 the syntheses of compounds 16-26 have been described.

Example 17. l,4-bis(4-methylphenyl)-2,5-bis(4-((trimethylsilyl)ethynyl)p henyl)-l,4- dihydropyrrolo[3,2-Z>] pyrrole (16)

Yellow solid. Yield 567 mg (15%). ^lb| R 0.78 (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 1 : 1). Mp 314-315°C (toluene, decomp.). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.26 (ΑΑ'ΧΧ', 4H), 7.14 (m, 12H), 6.36 (s, 2H), 2.37 (s, 6H), 0.23 (s, 18H); ¹ C NMR (125 MHz, CDC1 ₃ ) δ 137.5, 135.9, 130.0, 125.3, 21.2. HRMS (EI) calcd for C42H42N2S12: 630.2905[M ⁺ ], found:630.2905. (CH ₂ C1 ₂ , ε ^χ 10 ^"3 ) 393 (60) nm.

Example 18. 2,5-bis(2-bromophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydropy rrolo[3,2-Z>]pyrrole

(17)

Yellowish solid. Yield 291 mg (49%). ^[c] R _f = 0.68 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 239-241°C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.57 (dd, / = 8.1, 1.1 Hz, 2H), 7.28 (dd, / = 7.6, 1.7 Hz, 2H), 7.20 (dtJ = 7.5, 1.1 Hz, 2H), 7.10 (m, 10H), 6.45 (s, 2H), 2.31 (s, 6H). ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 137.4, 135.1, 134.7, 133.4, 133.1, 133.0, 129.8, 129.5, 128.6, 126.9, 124.4, 124.0, 96.3, 20.9. HRMS (EI) calcd for C ₃₂ H ₂₄ N ₂ Br ₂ : 594.0306 [M ⁺ ], found: 594.0305. Anal, calcd for C ₃₂ H ₂₄ Br ₂ N ₂ : C, 64.45; H, 4.06; Br,26.80; N, 4.70; found: C, 64.51 ; H, 4.24; Br, 26.78; N, 4.52. A _abs (CH ₂ Cl ₂ ,e x 10 ³ ) 306 (19) nm, 333 (18) nm. Example 19. 2,5-bis(2-methoxyphenyl)-l ,4-bis(4-methylphenyl)-l ,4-dihydropyrrolo [3,2- Z>]pyrrole (18)

Beige solid. Yield 224 mg (45%). ^[c] R _/= 0.61 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 286-289 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.31 (dd, / = 7.4, 1.3 Hz, 2H), 7.23 (dt, / = 8.8, 1.4 Hz, 2H), 7.13 (d, / = 8.2 Hz, 4H), 7.06 (d, / = 8.2 Hz, 4H), 6.92 (t, / = 7.4 Hz, 2H), 6.75 (d, / = 8.2 Hz, 2H), 6.37 (s, 2H), 3.37 (s, 6H), 2.31 (s, 6H). ¹³ C NMR ( 125 MHz, CDC1 ₃ ) δ 156.8, 138.6, 134.1, 131.8, 131.6, 130.0, 129.1, 128.4, 123.7, 123.4, 120.5, 111.0, 95.0, 54.9, 20.9. HRMS (EI) calcd for C ₃₄ H ₃₀ N ₂ O ₂ : 498.2307 [M ⁺ ], found: 498.2309. Anal, calcd for C ₃₄ H ₃₀ N ₂ O ₂ : C, 81.90; H, 6.06; N, 5.62; found: C, 81.62; H, 6.28; N, 5.39. A _abs (CH ₂ Cl ₂ ,e x 10 ³ ) 309 (23) nm, 338 (27) nm.

Example 20. 2,5-bis(2-(allyloxy)phenyl)- 1 ,4-bis(4-methylphenyl)- 1 ,4-dihydropyrrolo [3,2- Z>]pyrrole (19)

Beige solid. Yield 248 mg (45%). ^[c] R _/= 0.65 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 203-204 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.34 (dd, / = 7.5, 1.7 Hz, 2H), 7.20 (dt, / = 7.5, 1.7 Hz, 2H), 7.14 (d, / = 8.2 Hz, 4H), 7.05 (d, / = 8.2 Hz, 4H), 6.92 (dt, / = 7.4, 0.6 Hz, 2H), 6.76 (d, / = 8.2 Hz, 2H), 6.38 (s, 2H), 5.60 (m, 2H), 5.07 (m, 4H), 4.18 (m, 4H), 2.31 (s, 6H). ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 155.8, 138.7, 134.1, 133.8, 131.8, 130.1, 129.2, 128.3, 124.0, 123.3, 120.6, 116.8, 112.5 95.4, 68.9, 20.9. HRMS (EI) calcd for C ₃₈ H ₃₄ N ₂ 0 ₂ : 550.2620 [M ⁺ ], found: 550.2635. Anal, calcd for C ₃₈ H ₃₄ N ₂ 0 ₂ : C, 82.88; H, 6.22; N, 5.09; found: C, 83.05; H, 6.32; N, 5.09. A _abs (CH ₂ Cl ₂ ,e x 10 ³ ) 308 (24) nm, 336 (28) nm. Example 21. l,4-bis(4-methylphenyl)- 2,5-bis(4-(pentafluoro-A ⁶ -sulfanyl)phi

dihydropyrrolo [3,2-Z>] pyrrole (20)

Yellowish solid. Yield 241 mg (35%). ^[c] R _/= 0.70 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 322-324 °C (AcOEt, decomp.^H NMR (500 MHz, CDC1 ₃ ) δ 7.57 (d, / = 8.8 Hz, 4H), 7.23 (m, 8H), 7.16 (d, / = 8.2 Hz, 4H), 6.43 (s, 2H), 2.41 (s, 6H). ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 136.9, 136.7, 136.4, 134.6, 133.0, 130.1, 127.3, 125.8, 125.2, 95.6, 21.0. HRMS (EI) calcd for C ₃₂ H ₂₄ F ₁₀ N ₂ S ₂ : 690.1221 [M ⁺ ], found: 690.1230. Anal, calcd for C ₃₂ H ₂₄ F ₁₀ N ₂ S ₂ : C, 55.65; H, 3.50; F, 27.51 ;N, 4.06; S, 9.29; found: C, 55.64; H, 3.50; N, 4.12; F, 27.41 ; S, 9.18. A _abs (CH ₂ Cl ₂ ,e x 10 ³ ) 381 (41) nm.

Example 22. 1 ,2,4,5-tetrakis(4-(pentafluoro-A ⁶ -sulfanyl)phenyl)-l ,4-dihydropyrrolo [3,2- Z>]pyrrole (21)

Yellowish solid. Yield 238 mg (26%). ^[c] R _/= 0.67 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 329-331 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.83 (d, / = 8.2 Hz, 4H), 7.68 (d, / = 8.2 Hz, 4H), 7.34 (d, / = 8.1 Hz, 4H), 7.28 (d, / = 8.1 Hz, 4H) 6.54 (s, 2H); ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 151.2, 141.7, 135.7, 134.8, 132.5, 127.7, 127.6, 126.4, 124.6, 97.9. HRMS (EI) calcd for C ₃₀ H ₁₈ F ₂₀ N ₂ S ₄ : 914.0034 [M ⁺ ], found: 914.0029. Anal, calcd for C ₃₀ H ₁₈ F ₂₀ N ₂ S ₄ : C, 39.39; H, 1.98; F, 41.54; N, 3.06; S, 14.02; found: C, 39.57; H, 2.06; F, 41.32; N, 3.09; S, 14.18. A _abs (CH ₂ Cl ₂ ,e x 10 ³ ) 319 (23) nm, 376 (42) nm.

Example 23. l,4-bis(4-bromophenyl)-2,5-bis(4-cyanophenyl)-l,4-dihydropyr rolo[3,2- Z>]pyrrole(22)

Yellow solid. Yield 142 mg (23%). ^[c] R _{/ =} 0.56 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 351-353 °C (AcOEt, decomp H NMR (500 MHz, CDC1 ₃ ,) δ 7.55 (dd, / = 6.8, 1.9 Hz, 4H), 7.52 (dd, / = 6.8, 1.9 Hz, 4H), 7.27 (dd, J = 6.9, 2.0 Hz, 4H), 7.13 (dd, / = 6.9, 2.0 Hz, 4H) 6.54 (s, 2H) ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 138.2, 137.1, 135.2, 133.1, 132.8, 132.2, 128.0, 126.8, 120.3, 118.9, 109.8, 96.6. HRMS (EI) calcd for C ₃₂ H ₁₈ N ₄ Br ₂ : 615.9898 [M ⁺ ], found: 615.9924. Anal, calcd for C ₃₂ H ₁₈ Br ₂ N ₄ : C, 62.16; H, 2.93; Br, 25.85; N, 9.06; found: C, 62.11 ; H, 3.03; Br, 25.94; N, 9.15. A _abs (CH ₂ C1 ₂ , ε x 10 ³ ) 399 (50) nm.

Example 24. 2,5-bis(4-bromo-2-nitrophenyl)-l,4-bis(4-hexylphenyl)-l,4-di hydropyrrolo[3,2- fc]pyrrole (23)

Purple solid. Yield 208 mg (25%). ^M R _f = 0.75 (Si0 ₂ , CH ₂ Cl ₂ /hexanes, 1 : 1). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.86 (d, J = 2.0 Hz, 2H), 7.59 (dd, J = 8.3, 2.0 Hz, 2H), 7.28 (s, 2H), 7.11 (ΑΑ'ΧΧ', 4H), 7.07 (ΑΑ'ΧΧ', 4H), 6.32 (s, 2H), 2.66 - 2.52 (m, 4H), 1.60 (quin, J = 14.5 Hz, 4H), 1.31 (s, 12H), 0.89 (t, J = 6.8 Hz, 6H). ¹ C NMR (125 MHz, CDC1 ₃ ) δ 149.2, 141.3, 136.1, 135.3, 134.2, 132.0, 129.9, 129.5, 127.3, 127.3, 124.7, 121.0, 95.7, 35.6, 31.8, 31.4, 29.0, 22.8, 14.2. HRMS (EI) calcd for C ₄₂ H ₄₂ Br ₂ N ₄ 0 ₄ : 824.1588 [M ⁺ ], found: 824.1589. Anal, calcd for C ₄₂ H ₄₂ Br ₂ N ₄ 0 ₄ : C, 61.03; H, 5.12; N, 6.78; Br, 19.33; found: C, 60.94; H, 5.20; N, 6.69; Br, 19.29.

Example 25. 2,5-bis(benzo [Z>]thiophen-2-yl)-l ,4-bis(4-methylphenyl)-l ,4-dihydropyrrolo [3,2- b] pyrrole (24)

Purple solid. Yield 20 mg (4%). ^M R/= 0.72 (Si0 ₂ , AcOEt/hexanes, 4 : 6). ¾ NMR (500 MHz, CDC1 ₃ ) S 7.69 (d, J = 7.8, 2H), 7.54 (d, J = 7.2 Hz, 2H), 7.34 (ΑΑ'ΧΧ', 4H), 7.26 (ΑΑ'ΧΧ', 4H), 7.23 (dd, J = 4.4, 1.5 Hz; 2H), 7.21(dd, J = 7.1, 1.0 Hz, 2H), 6.77 (s, 2H), 6.45 (s, 2H), 2.44 (s, 6H). ¹ C NMR (125 MHz, CDC1 ₃ ) ^140.3, 139.0, 136.9, 136.8, 135.8, 132.8, 130.2, 130.2, 130.0, 126.1, 124. 2, 123.7, 123.1, 121.8, 120.2, 95.0, 21.2. HRMS (EI) calcd for C ₃₆ H ₂₆ N ₂ S ₂ : 550.1537 [M ⁺ ], found: 550.1551. Example 26. 2,5-di(benzofuran-2-yl)-l ,4-bis(4-methylphenyl)-l ,4-dihydropyrrolo [3,2-Z>] pyrrole

(25)

Orange solid. Yield 78 mg (15%). ^M ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.41 (ΑΑ'ΧΧ', 4H), 7.36 (m, 4H), 7.32 (ΑΑ'ΧΧ', 4H), 7.18 (m, 2H), 7.13 (dd, J = 7.6, 1.0 Hz, 2H), 6.68 (s, 2H), 5.96 (s, 2H), 2.49 (s, 6H). ¹ C NMR (125 MHz, CDC1 ₃ ) δ 153.9, 149.8, 137.4, 136.9, 133.5, 130.0, 129.2, 128.0, 126.4, 123.6, 122.7, 120.3, 110.6, 101.0, 93.7, 21.2. HRMS (ESI) calcd for ^ { ₂ ^ ₂ 0 ₂ : 518.1992 [M ⁺ ], found: 518.1992.

Example 27. l,4-bis(4-methylphenyl)-2,5-bis(thiazol-2-yl)-l,4-dihydropyr rolo[3,2-Z>]pyrrole (26)

Yellow solid. Yield 45 mg (10%). ^M ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.67 (d, J = 3.3 Hz, 2H), 7.31 (ΑΑ'ΧΧ', 4H), 7.27 (ΑΑ'ΧΧ', 4H), 7.08 (d, J = 3.3 Hz, 2H), 6.77 (s, 2H), 2.44 (s, 6H). ¹ C NMR (125 MHz, CDC1 ₃ ) δ 160.0, 142.6, 137.8, 136.2, 133.8, 130.1, 127.0, 117.6, 95.8, 21.4. HRMS (ESI) calcd for CzeH^Sz: 452.1139 [M ⁺ ], found: 452.1129

Example 28. General procedure for the synthesis of arylated 1 ,4-dihydropyrrolo [3 ,2-b] pyrroles

(27-34).

Parent l,4-dihydropyrrolo[3,2-6]pyrrole (0.25 mmol), aryl bromide (1 mmol), KOAc (1 mmol) and PdCl(C ₃ H ₅ )(dppb) (0.01 mmol) were placed in a 25 ml Schlenk flask, which was flushed with Argon prior to use. Then 8 ml of dry DMA was added and resulting mixture was stirred at 150 °C for 3 days. Product was purified by means of flash column chromatography, and then recrystallized from toluene or ethyl acetate. Obtained crystals were dried under reduced pressure.

1 ₌ CN

R ₂ = Me The examples 29-36 present synthetic results of applied procedure - compounds 27-34.

Example 29. 2,5-bis(4-cyanophenyl)-3-(9,9-dioctyl-9H-fluoren-3-yl)-l,4-b is(4-methylphenyl)- dihydropyrrolo[3,2-Z>] pyrrole (27)

Yellow solid. Product was purified by means of flash column chromatography (SiO _z , CH ₂ Cl ₂ /hexanes 1: 1). Yield 66 mg (30%). R _{/ =} 0.66 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 228- 231°C (toluene). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.62 (d, /= 7.2 Hz IH), 7.42 (ΑΑ'ΧΧ', 2H), 7.33 (m, IH), 7.29 (m, 3H), 7.27 (m, IH), 7.21 (m, 5H), 7.12 (ΑΑ'ΧΧ', 2H), 7.07 (d, / = 8.4 Hz, 2H), 6.86 (s, IH), 6.79 (s, 4H), 6.64 (dd, /= 7.7, 1.3 Hz, IH), 6.54 (s, IH), 2.40 (s, 3H), 2.25 (s, 3H), 1.80 (m, 2H), 1.63 (m, 2H), 1.21 (m, 4H), 1.15 (m, 8H), 1.04 (m, 4H), 0.99 (m, 4H), 0.82 (t, /= 7.0 Hz, 6H), 0.49 (quin, /= 7.8 Hz, 4H). ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 150.7, 150.2, 140.9, 139.4, 137.8, 136.9, 136.2, 135.6, 131.9, 131.3, 130.8, 130.0, 129.2, 127.9, 127.1, 125.3, 122.8, 119.4, 118.6, 112.3, 109.0, 94.1, 54.8, 40.3, 31.8, 30.0, 29.5, 29.3, 23.7, 22.6, 21.0, 14.1. HRMS (ESI) calcd for C ₆₃ H ₆₄ N ₄ :876.5131 [M ⁺ ], found: 876.5124. Anal, calcd for C ₆₃ H ₆₄ N ₄ : C, 86.26; H, 7.35; N, 6.39; found: C, 86.02; H, 7.38; N, 6.30. A _abs (CH ₂ C1 ₂ , ε x 10 ³ ) 404 (40) nm.

Example 30. 2,5-bis(4-cyanophenyl)-l ,4-bis(4-methylphenyl)-3-(4-nitrophenyl)- dihydropyrrolo[3,2-Z>] pyrrole (28)

Orange solid. Product was purified by means of flash column chromatography (Si0 ₂ , CH ₂ Cl ₂ /hexanes 1: 1). Yield 36 mg (24%). R _/= 0.51 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 344- 346 °C (toluene). ¾ NMR (500 MHz, CDCI ₃ ) δ 7.80 (ΑΑ'ΧΧ' , 2H), 7.44 (ΑΑ'ΧΧ', 2H), 7.39 (AA'XX' ,2H), 7.20 (t, /= 8.5 Hz, 4H), 7.08 (ΑΑ'ΧΧ', 2H), 7.03 (ΑΑ'ΧΧ', 2H), 6.95 (d, /= 8.0 Hz,2H), 6.84-6.81 (m, 2H), 6.51 (s, IH), 2.40 (s, 3H), 2.34 (s, 3H). ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 145.8, 140.4, 138.0, 137.4, 136.9, 136.2, 136.1, 136.0, 135.9, 132.0, 131.9, 131.8, 131.1, 130.7, 130.1, 129.6, 128.0, 127.5, 125.5, 124.8, 122.7, 119.0, 118.6, 110.3, 109.4, 109.0, 94.5, 21.1, 21.0. HRMS (EI) calcd for ^Η ₂₇ Ν ₅ 0 ₂ : 609.2165 [M+], found: 609.2184. A _abs (CH ₂ Cl ₂ , ε x 10 ³ ) 393 (40) nm. Example 31. 2,5-bis(4-cyanophenyl)-l ,4-bis(4-methylphenyl)-3,6-bis-(4-nitrophenyl)- dihydropyrrolo[3,2-Z>] pyrrole (29)

Orange solid. Product was purified by means of flash column chromatography (SiO _z , CH ₂ Cl ₂ /hexanes 2: 1) Yield 97 mg (53%). R _/= 0.42 (Si0 ₂ , AcOEt/hexanes, 1:4). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.79(d, 4H), 7.35 (d, 4H), 6.98 (d, 4H), 6.91 (d, 4H), 6.82( d, 4H), 6.77(d, 4H), 2.32 (s, 6H). ¹³ C NMR (125 MHz, CDC1 ₃ ) δ 145.8, 140.0, 138.2, 135.8, 135.2, 133.3, 131.8, 131.4, 131.0, 129.5, 129.2, 127.6, 124.8, 122.8, 118.5, 110.6, 108.0, 21.1. HRMS (EI) calcd for C^ _Q N^ [M ⁺ ]= 730.2329, found [M ⁺ ]= 730.2345. Anal, calcd for C^oN^: C, 75.60, H, 4.14, N 11.50 found: C, 75.56, H, 4.20, N, 11.41. A _abs (CH ₂ Cl ₂ , ε x 10 ³ ) 381 (45) nm.

Example 32. 2,5-bis(4-cyanophenyl)-l ,4-bis(4-methylphenyl)-3,6-bis(4-(pentafluoro-A ⁶ - sulf anyl)phenyl)- 1 ,4-dihydr opyrr olo [3,2-Z>] pyrrole (30)

Yellow -greenish solid. Product was purified by means of flash column chromatography (Si0 ₂ , CH ₂ Cl ₂ /hexanes 1: 1-3: 1). Yield 78 mg (35%). R _/= 0.56 (Si0 ₂ , AcOEt/hexanes, 1:4). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.36(ΑΑ'ΧΧ', 4H), 7.30 (ΑΑ'ΧΧ', 4H), 7.01 (ΑΑ'ΧΧ', 4Η), 6.86 (d, / = 8.0 Hz, 4H), 6.78 (d, J = 8.5 Hz, 4H), 6.70 (AA'XX',4H), 2.29 (s, 6H). ¹ C NMR (125 MHz, CDC1 ₃ ) δ 137.8, 136.7, 135.9, 135.2, 132.3, 131.8, 131.1, 130.4, 129.5, 129.4, 127.4, 125.2, 125.1, 118.7, 110.2, 108.0, 20.8. HRMS (EI) calcd for C ₄ 6H ₃ oN ₄ F ₁₀ S2: 892.1752 [M+], found: 892.1734. (CH ₂ C1 ₂ , ε * 10 ^"3 ) 395 (33) nm.

Example 33. 2,5-bis(4-cyanophenyl)-l ,4-bis(4-methylphenyl)-3-(pyridin-3-yl)-l ,4- dihydropyrrolo[3,2-Z>] pyrrole (31)

Yellow solid. Product was purified by means of flash column chromatography (SiO _z , CH ₂ Cl ₂ /MeOH 95:5). Yield 30 mg (21%). R _f = 0.71 (Si0 ₂ , CH ₂ Cl ₂ /MeOH, 95:5). Mp 319- 320 °C (toluene, decomp.). ¾ NMR (500 MHz, CDC1 ₃ ) S 8.34 (d, /= 2.0 Hz, 1H), 8.02 (s, 1H), 7.43 (d, 7=7.8 Hz, 2H), 7.36 (d, J = 7.8 Hz, 2H) 7.20 (m, 4H), 7.09 (d, J = 7.6 Hz, 2H), 7.01(m, 3H), 6.91 (m, 3H), 6.80 (d, J = 7.5 Hz, 2H), 6.52 (s, 1H), 2.39 (s, 3H), 2.31 (s, 3H). ¹ C NMR (125 MHz, CDC1 ₃ ) δ 150.0, 147.0, 137.9, 137.6, 137.5, 136.6, 136.3, 136.2, 136.0, 135.6, 132.1, 131.9, 131.8, 131.7, 131.3, 131.0, 130.1, 129.6, 129.3, 127.9, 127.3, 125.4, 122.4, 119.0, 118.8, 109.9, 109.2, 107.2, 94.5, 21.1, 21.0. HRMS (EI) calcd for C ₃₉ H ₂₇ N ₅ : 565.2266 [M+], found: 565.2280. _s (CH ₂ Ci ₂ , ε ^χ 10 ^"3 ) 395 (33) nm.

Example 34. 2,5-bis(4-cyanophenyl)-l ,4-bis(4-methylphenyl)-3,6-di(pyridin-3-yl)-l ,4- dihydropyrrolo[3,2-Z>] pyrrole (32)

Yellow solid. Product was purified by means of flash column chromatography (SiO _z , CH ₂ Cl ₂ /MeOH 95:5). Yield 76 mg (47%). R _j = 0.55 (Si0 ₂ , CH ₂ Cl ₂ /MeOH, 95:5). Mp 345- 347 °C (toluene, decomp.). ¾ NMR (500 MHz, CDC1 ₃ ) δ 8.33(d, J = 3.0 Hz,2H), 8.01 (s, 2H), 7.32 (d, J= 8.2 Hz,4H), 7.01 (d, J = 7.6 Hz, 2H), 6.97 (d, J= 8.2 Hz, 4H), 6.89 (m, 6H), 6.75 (d, J = 8.0 Hz, 4H), 2.31 (s, 6H). ¹ C NMR (125 MHz, CDC1 ₃ ) S 151.0, 147.0, 137.8, 137.6, 136.1, 135.1, 133.1, 131.7, 131.2, 129.5, 129.4, 129.2, 127.4, 122.5, 118.7, 110.1, 106.1, 21.1. HRMS (EI) calcd for C ₄₄ H ₃₀ N ₆ : 642.2532 [M+], found: 642.2521. _s (CH ₂ Ci ₂ , ε ^χ 10 ^"3 ) 396 (36) nm.

Example 35. 2,3,5-tris(4-cyanophenyl)-l,4-bis(4-methylphenyl)-l,4-dihydr opyrrolo[3,2-Z>]pyrrole (33)

Yellow solid. Product was purified by means of flash column chromatography (Si0 ₂ , CH ₂ Cl ₂ /hexanes 1: 1-3: 1). Yield 71 mg (48%). R _{/ =} 0.41 (Si0 ₂ , AcOEt/hexanes, 1:4). Mp 325- 326 °C (toluene). ¾ NMR (500 MHz, CDC1 ₃ ) S 7.43 (d, J = 8.2 Hz, 2H), 7.38 (d, J= 8.2 Hz, 2H), 7.20 (m, 6H), 7.07 (d, J = 8.1 Hz, 2H), 7.00 (d, J = 8.2 Hz, 2H), 6.94 (d, J = 7.9 Hz, 2H), 6.79 (m, 4H), 2.39 (s, 3H), 2.36 (s, 3H). ¹ C NMR (125 MHz, CDC1 ₃ ) δ 138.3, 137.8, 136.8, 136.3, 136.1, 136.0, 135.9, 131.9, 131.8, 131.7, 131.2, 131.1, 130.7, 130.1, 129.5, 128.0, 127.4, 125.4, 119.0, 118.7, 110.1, 109.5, 109.4, 109.3, 94.5, 21.1, 21.0. HRMS (EI) calcd for C ₄ iH ₂₇ N ₅ : 589.2266 [M+], found: 589.2259. Anal, calcd for C ₄ iH ₂₇ N ₅ : C, 83.51; H, 4.62; N, 11.88; found: C, 83.47; H, 4.63; N, 11.72. (CH ₂ C1 ₂ , ε ^χ 10 ^"3 ) 400 (43) nm.

Example 36. 2,5-bis(4-cyanophenyl)-3-(4-methoxyphenyl)-l,4-bis(4-methylp henyl)-l,4- dihydropyrrolo[3,2-Z>] pyrrole (34)

Yellow solid. Product was purified by means of flash column chromatography (Si0 ₂ , AcOEt/hexanes 1 :4). Yield 50 mg (34%). R _f = 0.45 (Si0 ₂ , AcOEt/hexanes, 1 :4). Mp 298- 300 °C (toluene). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.42 (d, J = 8.3 Hz, 2H), 7.33 (d, J = 8.3 Hz,2H), 7.20 (d, J = 8.3 Hz, 2H), 7.17 (d, J = 8.3 Hz, 2H), 7.08 (d, J = 8.1 Hz, 2H), 7.03 (d, J = 8.2 Hz, 2H), 6.89 (d, J = 8.0 Hz, 2H), 6.78 (d, J = 8.1 Hz,2H), 6.62 (d, J = 8.5 Hz, 2H), 6.52 (d, J = 6.8 Hz, 2H), 6.51 (s, 1H), 3.75 (s, 3H), 2.39 (s, 3H), 2.32 (s, 3H). ¹ C NMR (125 MHz, CDC1 ₃ ) δ 158.1, 137.8, 137.1, 136.8, 136.7, 136.1, 135.8, 135.6, 131.9, 131.7, 131.7, 131.6, 131.4, 130.9, 130.0, 129.2, 127.9, 127.3, 125.3, 125.0, 113.1, 111.3, 109.1, 108.9, 94.6, 55.2, 21.1, 21.0. HRMS (EI) calcd for C ₄ iH ₃ oN ₄ 0: 594.2420 [M+], found: 594.2430. _s (CH ₂ Ci ₂ , ε ^χ 10 ^"3 ) 400 (43) nm.

Example 37. General procedure for the synthesis of 2,5-bis(arylethynyl)-l,4-bis(aryl)-l,4- dihydropyrrolo[3,2-Z>] pyrroles (35-39).

An oven-dried 25 ml Schlenk flask was charged with l,4-bis(4-methylphenyl)-2,5-bis(4- ((trimethylsilyl)ethynyl)phenyl)-l,4-dihydropyrrolo[3,2-6]py rrole (16, 20 mg, 3.17 x 10 ^s mol), PdCl ₂ (PPh ₃ ) ₂ (2.2 mg, 3.17 x 10 ⁶ mol), Cul (0.6 mg, 3.17 x 10 ⁶ mol) and bromo- or iodoarene (6.317 x 10 ⁵ mol). Then anhydrous THF (0.5 ml) was added, followed by Et ₃ N (0.5 ml, 3.6 mmol). Reaction mixture were deoxygenated by freeze-pump-thaw cycles and purged with argon. TBAF (21 mg, 7.92 x 10 ⁶ mol) was added, and the reaction mixture was stirred for 16 h at room temperature under argon atmosphere. The crude mixture was filtered through celite and the solvent was distilled off. Purification using DCVC method afforded pure product. The examples 38-42 present synthetic results of applied procedure - compounds 35-39.

Example 38. 2,5-bis(4-(4-cyanophenylethynyl)phenyl)-l ,4-bis(4-methylphenyl)-l ,4- dihydropyrrolo[3,2-Z>] pyrrole (35)

Product was purified by means of DCVC method (SiO _z , hexanes/CH ₂ Cl ₂ , 4: 1) afforded pure product as a yellow solid, 12 mg (56%). R _f = 0.27 (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 1: 1). Mp 313-314°C (AcOEt, decomp.). ¾ NMR (500 MHz, CDC1 ₃ ) S 7.61 (ΑΑ'ΧΧ', 4H), 7.57 (ΑΑ'ΧΧ', 4H), 7.38 (ΑΑ'ΧΧ' , 4H), 7.21 (ΑΑ'ΧΧ', 4Η), 7.19 (m, 8Η), 6.42 (s, 2H), 2.39 (s, 6H); ¹³ C NMR ( 125 MHz, CDC1 ₃ ) ό 137.5, 136. 1 , 135.7, 134.5, 132.9, 132.2, 132. 1 , 131.8, 130.1 , 128.5, 127.9, 125.4, 1 19.6, 1 18.6, 1 1 1.5, 95.2, 88.5, 21.2. HRMS (EI) calcd for C ₅₀ H ₃₂ N ₄ : 688.2627 [M ⁺ ], found: 688.2596.

b _* (CH ₂ C1 ₂ , ε x 10 ³ ) 428 (70) nm.

Example 39. 2,5-bis(4-(4-pentafluorothiophenyl)ethynylphenyl)-l ,4-bis(4-methylphenyl)-l ,4- dihydropyrrolo[3,2-Z>] pyrrole (36)

Purification using DCVC method (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 4: 1) afforded pure product as a yellow solid, 6 mg (21 %). R _{/ =} 0.72 (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 1 : 1). Mp 207-208°C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) S 7.65 (ΑΑ'ΧΧ', 4H), 7.48 (ΑΑ'ΧΧ', 4H), 7.33 (ΑΑ'ΧΧ', 4H), 7.14 (ΑΑ'ΧΧ' , 4Η), 7. 13 - 7.08 (m, 8Η), 6.36 (s, 2H), 2.32 (s, 6H); ¹ C NMR (125 MHz, CDC1 ₃ ) S 137.3, 135.9, 135.5, 134.2, 132.6, 131.6, 131.5, 129.9, 127.7, 127.1, 126.0, 125.2, 1 19.5, 95.0, 92.7, 87.9, 29.7, 21.0. HRMS (EI) calcd for C^^NA: 890. 1847[M ⁺ ], found: 890.1843. A _abs (CH ₂ C1 ₂ , ε x 10 ³ ) 418 (45) nm. Example 40. 2,5-bis(4-(4-trifluoromethyl)ethynylphenyl)-l ,4-bis(4-methylphi

dihydropyrrolo[3,2-Z>] pyrrole 37)

Purification using DCVC method (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 6: 1) afforded pure product as a orange solid, 4 mg(15%). R = 0.76 (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 1 : 1). Mp 347-348 °C (AcOEt, decomp.). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.59 (s, 8H), 7.39 (ΑΑ'ΧΧ', 4H), 7.19 (m, 12H), 6.42 (s, 2H), 2.38 (s, 6H). ¹ C NMR (125 MHz, CDC1 ₃ ) δ 137.5, 136.0, 131.9, 130. 1, 125.4, 125.4, 21.2. HRMS (EI) calcd for C ₅₀ H ₃₂ F ₆ N ₂ : 774.2470 [M ⁺ ], found: 774.2461. (CH ₂ C1 ₂ , ε ^χ 10 ^"3 ) 414 (62) nm.

Example 41. 2,5-bis(4-(3,5-di(trifluoromethyl)ethynylphenyl)-l ,4-bis(4-methylphenyl)-l ,4- dihydropyrrolo[3,2-Z>] pyrrole (38)

Purification using DCVC method (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 8: 1) afforded pure product as ayellow solid, 10 mg (33%). R _f = 0.78 (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 1 : 1). Mp 316-317 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.92 (s, 4H), 7.80 (s, 2H), 7.40 (ΑΑ'ΧΧ', 4H), 7.23 (ΑΑ'ΧΧ', 4H), 7.20 (m, 8H), 6.45 (s, 2H), 2.39 (s, 6H); ¹ C NMR ( 125 MHz, CDC1 ₃ ) δ 137.4, 136. 1, 134.6, 132.9, 132.2, 132.0, 131.8, 131.4, 130. 1, 127.9, 125.9, 125.3, 124.2, 122.0, 1 19. 1, 95.2, 93.3, 87.0, 21.2. HRMS (EI) calcd for C ₅₂ H ₃₀ F ₁₂ N ₂ : 910.2215 [M ⁺ ], found: 910.2188. A _abs (CH ₂ C1 ₂ , ε ^χ 10 ^"3 ) 421 (67) nm

Example 42. 2,5-bis(4-(methoxy)ethynylphenyl)-l ,4-bis(4-methylphenyl)-l ,4-dihydropyrrolo [3,2- Z>]pyrrole(39)

Purification using DCVC method (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 3 : 1) afforded pure product as ayellow solid, 7 mg (30%). R _f = 0.44 (Si0 ₂ , hexanes/CH ₂ Cl ₂ , 1 : 1). Mp 315-316 °C (AcOEt). ¾ NMR (500 MHz, CDC1 ₃ ) δ 7.44 (ΑΑ'ΧΧ', 4H), 7.35 (ΑΑ'ΧΧ', 4H), 7. 18 (s, 12H), 6.87 (ΑΑ'ΧΧ', 4H), 6.40 (s, 2H), 3.82 (s, 6H), 2.38 (s, 6H); ^1J C NMR (125 MHz, CDC1 ₃ ) δ 159.7, 137.5, 135.8, 133.1, 131.3, 123.0, 129.2, 128.4, 127.8, 125.5, 125.3, 114.1, 55.5, 21.2. HRMS (EI) calcd for C ₅ oH ₃₈ N ₂ 0 ₂ : 698.2933 [M ⁺ ], found: 698.2955.A _abs (CH ₂ C1 ₂ , ε ^χ 10 ^"3 ) 401 (71) nm.

Example 43. Optical properties of compounds synthesized according to the present invention.

Optical measurements were performed for compounds synthesized according to the present invention. For this purpose each compound was dissolved in CH ₂ C1 ₂ , unless otherwise noted, and absorption spectra were measured. The same solutions were exposed to monochromatic light with wavelength 325 - 345 nm and emission spectra were measured. Comparison with reference spectrum (quinine bisulfate (VI) in H ₂ S0 ₄ , 0.5 M) gave the fluorescence quantum yield coefficient. All the measurements were performed at room temperature. Results are shown in Table 1.

Table 1. Spectroscopic properties of selected compounds.

Stokes Molar absorption Fluorescence Cpd labs [nm] /l _em [nm] Shift coefficient quantum yield

[cm ¹ ! e _max [M ^"1 cm ^"1 ! CZ½

2 348 410 4300 37 000 0.37

3 377 443 4000 14 000 0.51

5 405 459 3000 54 000 0.24

6 368 462 5500 33 000 0.17

9W 348 412 4500 36 000 0.52

11 400 455 3000 49 000 0.78

12 345 400 4000 34 000 0.57

13 360 - - 41 000 -

19 336 414 5600 28 000 0.62

22 399 454 3000 50 000 0.86

27 404 472 3600 40 000 0.57

29 381 - - 45 000 -

30 395 463 3700 33 000 0.63

32 396 465 3800 36 000 0.64

33 400 474 3900 43 000 0.48

35 428 549 5200 70 000 0.22

36 418 523 4800 45 000 0.16

37 414 511 4600 62 000 0.42

38 421 522 4600 67 000 0.37

39 401 479 4100 71 000 0.53

[a] spectra measured in toluene

Fig. 1 shows fluorescence of selected compounds in solutions.

Example 44. Electrochemical properties of compound according to the invention.

Electrochemistry of two compounds (19 and 32) has been studied via cyclic voltammetry (Table 2, Fig. 2-3). It was shown that some of these compounds have interesting behavior such as low oxidation potential and large HOMO-LUMO gap. This can be advantageous in such applications as bulk- heterojunction solar cells, organic field-effect transistors etc. Table 2. Electrochemical data for compounds 19 and 32 vs. Fc/Fc ⁺ ).

Fig. 2 shows a cyclic voltammetry for compound 19 and Fig. 3 the cyclic voltammetry for compound 32.