Supporting Information. for. Rapid pseudo five-component synthesis of. intensively blue luminescent 2,5-di(hetero)arylfurans
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1 Supporting Information for Rapid pseudo five-component synthesis of intensively blue luminescent 2,5-di(hetero)arylfurans via a Sonogashira Glaser cyclization sequence Fabian Klukas, Alexander Grunwald, Franziska Menschel, and Thomas J. J. Müller* Address: Heinrich-Heine Universität Düsseldorf, Institut für Organische Chemie und Makromolekulare Chemie, Universitätsstraße 1, D Düsseldorf, Germany Thomas J.J.Müller - ThomasJJ.Mueller@uni-duesseldorf.de *Corresponding author Experimental procedures, spectroscopic and analytical data of all compounds 2. s1
2 Table of Contents 1. General considerations... s3 2. General procedure for optimization studies... s5 3. General procedure for the Sonogashira Glaser cyclization sequence... s6 4. Analytical data of compounds 2a 2o... s7 5. UV-absorption and fluorescence data of compounds 2a 2o... s22 6. NMR spectra of compounds 2a 2o... s30 7. CV data of compounds 2a 2o... s60 8. xyz-coordinates and dihedral angles of compounds 2a 2o... s66 s2
3 1. General considerations All cross coupling reactions were carried out in oven-dried 80 ml microwave vessels (CEM Corporation) by using septa and syringes under nitrogen atmosphere. Commercial-grade reagents were used as supplied without further purification and were purchased from Sigma-Aldrich Chemie GmbH, ABCR GmbH & Co. KG, Alfa Aesar GmbH & Co. KG, and Merck Serono KGaA. The purification of products was performed on silica gel 60 ( mm) from Macherey-Nagel Düren by using the flash technique under a pressure of 1.5 bar. The crude mixtures were adsorbed on Celite 545 ( mm) from Merck Serono KGaA Darmstadt before chromatographic purification. The reaction progress was monitored qualitatively by TLC silica gel 60 F254 aluminium sheets obtained by Merck Serono KGaA Darmstadt. The spots were detected with UV light at 254 nm and by using aqueous potassium permanganate solution. 1 H, 13 C, and 135-DEPT NMR spectra were recorded on a Bruker Avance III 600 spectrometer. CDCl 3 and DMSO-d 6 were used as deuterated solvents. The resonances of the residues of nondeuterated solvent were locked as internal standards (CDCl 3 : 1 H 7.26, 13 C 77.2; DMSO-d 6 : 1 H 2.50, 13 C 39.52). The multiplicities of signals were abbreviated as follows: s: singlet; d: doublet; t: triplet; dd: doublet of doublets and m: multiplet. The type of carbon atoms was determined on the basis of 135-DEPT NMR spectra. EI mass spectra were measured on a Finnigan MAT 8200 or Shimadzu GC-2010/QP-2010 spectrometer. IR spectra were obtained on Bruker Vector 22 FTIR. The intensity of signals is abbreviated as follows: s (strong), m (medium) and w (weak). The melting points (uncorrected) were measured on a Büchi Melting Point B-540. Combustion analyses were carried out on Perkin Elmer Series II Analyser 2400 in the microanalytical laboratory of the Institut für Pharmazeutische and Medizinische Chemie at the Heinrich Heine-Universität Düsseldorf. The UV vis spectra were recorded with a Perkin Elmer Spectrometer (Lambda 19). The emission data were carried out on Perkin Elmer Luminescence Spectrometer (LS55). The quantum yield was determined as followed: ( ) ( ) [1] with p-terphenyl ( f = 93 % in cyclohexane) [2] or coumarin 1 ( f = 73 % in EtOH) [3] as a reference. s3
4 Cyclic voltammetry experiments were performed with a 263A E&G Princeton Applied Research device under argon in dry and degassed dichloromethane at T = 293 K at scan rates of 100, 250, 500 and 1000 mvs 1. The electrolyte was tetrabutylammonium hexafluorophosphate at a concentration of c = 0.1 mol L 1. The working electrode was a 1 mm platinum disk, the counter electrode was a platinum wire and the reference electrode was a silver/silverchloride electrode filled with 3 M potassium chloride solution. The potentials were calibrated using [FeCp 2 ]/[FeCp 2 ] + (E 0/+1 0 = 450 mv) [4] as an internal potential standard. Computational support and infrastructure was provided by the "Center for Information and Media Technology" (ZIM) at the Heinrich-Heine-Universität Dü. The geometries of the ground state structures were optimizied on the DFT level of theory (B3LYP/6-311G(d,p) [5,6,7,8,9]) as implemented in Gaussian09 [10]. s4
5 2. General procedure for optimization studies A mixture of iodobenzene 3a (101 mg, 0.50 mmol), H 2 O (18.0 mg, 1.00 mmol) and potassium hydroxide (56.1 mg, 1 mmol) was dissolved in DMSO (2.00 ml) in a 10 ml microwave vessel equipped with a stirring bar and a septum. The mixture was heated in the microwave cavity at 130 C for 1 h. After cooling to room temperature the mixture was extracted with methylene chloride (100 ml) and brine (250 ml). The organic phase was dried with anhydrous Na 2 SO 4 and the solvents were removed under reduced pressure. The residue was absorbed on Celite and purified by column chromatography on silica gel with n-hexane. s5
6 3. General procedure for the Sonogashira Glaser cyclization sequence In manner similar to [11] A mixture of a (hetero)aryl iodide 3 (2.00 mmol), PdCl 2 (PPh 3 ) 2 (28.1 mg, 0.04 mmol, 2 mol %), and CuCl (7.92 mg, 0.08 mmol, 4 mol %) was dissolved in DMSO (2.00 ml) in a 80 ml microwave vessel equipped with a stirring bar and a septum and was degassed with N 2 for 5 min. After addition of trimethylsilylacetylene (0.42 ml, 3.00 mmol) and dry triethylamine (0.55 ml, 4.00 mmol) the solution was stirred at room temperature for 1 h. Then, KF (232 mg, 4.00 mmol) was added and the reaction mixture was vigorously stirred under air in the open reaction vessel at room temperature for 16 h. After the addition of H 2 O (144 mg, 8.00 mmol), potassium hydroxide (449 mg, 16 mmol), and DMSO (14.0 ml) the mixture was heated in the microwave cavity at 130 C for 1 h. After cooling to room temperature the mixture was extracted with methylene chloride (300 ml) and brine (500 ml). The organic phase was dried with anhydrous Na 2 SO 4 and the solvents were removed under reduced pressure. The residue was absorbed on Celite and purified by column chromatography on silica gel with n-hexane or n- hexane/thf as eluent. s6
7 4. Analytical data of compounds 2a 2o 2,5-Diphenylfuran (2a) [12] The synthesis was carried out according to the general procedure with 408 mg (2.00 mmol) of iodobenzene (3a) (Alfa Aesar). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 96.0 mg (0.44 mmol, 44 %) of the desired product as colorless crystals. R f : = 0.31 (n-hexane). Mp 84 C (66-68 C [12]). 1 H NMR (DMSO-d 6, 600 MHz): = 7.08 (s, 2 H), 7.31 (t, 3 J = 7.4 Hz, 2 H), 7.46 (t, 3 J = 7.8 Hz, 4 H), 7.82 (d, 3 J = 7.3 Hz, 4 H). 13 C NMR (DMSO, 150 MHz): = (CH), (CH), (CH), (CH), (C quat ), (C quat ). GC-MS (m/z (%)): 220 (M +, 100), 191 (13), 115 ((M-C 7 H 5 O) +, 41), 105 ((C 7 H 5 O) +, 22), 89 (14), 77 ((C 6 H 5 ) +, 51), 63 (13), 51 (22); IR (KBr): = 1479 (w) cm -1, 1446 (w), 1155 (w), 1022 (m), 925 (w), 910 (w), 794 (m), 756 (s), 689 (s), 671 (m). Anal. calcd for C 16 H 12 O (220.3): C 87.25, H 5.49; Found: C 87.09, H UV vis (CH 2 Cl 2 ): max ( ): 327 nm (35000 L mol - 1 cm -1 ), 342 (22000). Fluorescence (CH 2 Cl 2 ): max : 358 nm. Stokes hi t Δ = 3800 cm -1. Quantum yield: f = 83 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [2]). Cyclic voltammetry (CH 2 Cl 2 ): E 1/2 0/+1 = 1.25 V. s7
8 2,5-Di-o-tolylfuran (2b) The synthesis was carried out according to the general procedure with 436 mg (2.00 mmol) of o-iodotoluene (3b) (Alfa Aesar). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 126 mg (0.51 mmol, 51%) of the desired product as colorless solid. R f = 0.31 (n-hexane). Mp 70 C. 1 H NMR (DMSO-d 6, 600 MHz): = 2.50 (s, 6 H), 6.87 (t, 3 J = 1.9 Hz, 2 H), 7.22 (t, 3 J = 7.4 Hz, 2 H), 7.28 (t, 3 J = 6.9 Hz, 4 H), 7.76 (d, 3 J = 7.2 Hz, 2 H). 13 C NMR (DMSO, 150 MHz): = 21.7 (CH 3 ), (CH), (CH), (CH), (CH), (C quat ), (CH), (C quat ), (C quat ); GC-MS (m/z (%)): 248 (M +, 100), 128 ((C 10 H 8 ) +, 40), 119 ((M-C 10 H 9 ) +, 69), 91 ((C 7 H 7 ) +, 71), 77 ((C 6 H 5 ) +, 15), 65 (29); IR (KBr): = 1481 (w) cm -1, 1458 (w), 1436 (w), 1030 (w), 928 (w), 789 (w), 756 (s), 721 (m), 671 (w);. Anal. calcd for C 18 H 16 O (248.3): C 87.05, H 6.49; Found: C 86.86, H 6.28; UV vis (CH 2 Cl 2 ): max ( ): 314 nm (23000 L mol -1 cm -1 ), 342 (9000). Fluorescence (CH 2 Cl 2 ): max : 359 nm. Stokes shift Δ = 5200 cm -1. Quantum yield: f = 59 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [2]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.19 V. s8
9 2,5-Di-m-tolylfuran (2c) [12] The synthesis was carried out according to the general procedure with 436 mg (2.00 mmol) of m-iodotoluene (3c) (Sigma-Aldrich). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 160 mg (0.65 mmol, 65%) of the desired product as colorless solid. R f : = 0.24 (n-hexane)). Mp 83 C (colorless oil [12]); 1 H NMR (DMSO-d 6, 600 MHz): = 2.37 (s, 6 H), 7.03 (s, 2 H), 7.12 (d, 3 J = 7.5 Hz, 2 H), 7.33 (t, 3 J = 7.6 Hz, 2 H), 7.61 (d, 3 J = 7.9 Hz, 2 H), 7.64 (s, 2 H). 13 C NMR (DMSO, 150 MHz): = 21.0 (CH 3 ), (CH), (CH), (CH), (CH), (CH), (C quat ), (C quat ), (C quat ). GC-MS (m/z (%)): 248 (M+, 100), 128 ((C 10 H 8 ) +, 20), 119 ((M- C 10 H 9 ) +, 12), 91 ((C 7 H 7 ) +, 36), 77 ((C 6 H 5 ) +, 11), 65 (21). IR (KBr): = 1476 (w) cm -1, 1260 (w), 1092 (w), 1026 (m), 779 (s), 698 (m). Anal. calcd for C 18 H 16 O (248.3): C 87.05, H 6.49; Found: C 86.86, H UV vis (CH 2 Cl 2 ): max ( ): 331 nm (33000 L mol -1 cm -1 ), 348 (20000). Fluorescence (CH 2 Cl 2 ): max : 360 nm. Stokes shift Δ = 3800 cm -1. Quantum yield: f = 72 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [2]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.19 V. s9
10 2,5-Di-p-tolylfuran (2d) [12] The synthesis was carried out according to the general procedure with 436 mg (2.00 mmol) of p-iodotoluene (3d) (Sigma-Aldrich). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 100 mg (0.40 mmol, 40%) of the desired product as colorless solid. R f.: = 0.31 (n-hexane). Mp 168 C ( C [12]). 1 H NMR (DMSO-d 6, 600 MHz): = 2.33 (s, 6 H), 6.97 (s, 2 H), 7.25 (d, 3 J = 8.4 Hz, 4 H), 7.69 (t, 3 J = 8.4, 4 H). 13 C NMR (DMSO, 150 MHz): = 20.9 (CH), (CH), (CH), (C quat ), (CH), (C quat ), (C quat ). GC-MS (m/z (%)): 248 (M+, 100), 205 (6), 129 ((C 10 H 7 ) +, 15), 119 ((M-C 10 H 9 ) +, 11), 91 ((C 7 H 7 ) +, 24), 77 ((C 6 H 5 ) +, 7), 65 (14); IR (KBr): = 2911 (w) cm -1, 1912 (w), 1501 (m), 1487 (m), 1375 (w), 1287 (w), 1209 (w), 1113 (w), 1063 (w), 1017 (m), 928 (m), 824 (s), 791 (s), (716 (m), 673 (m). Anal. calcd for C 18 H 16 O (248.3): C 87.05, H 6.49; Found: C 87.27, H UV vis (CH 2 Cl 2 ): max ( ): 331 nm (33000 L mol -1 cm -1 ), 348 (20000). Fluorescence (CH 2 Cl 2 ): max : 360 nm. Stokes shift: Δ = 3800 cm -1 ). Quantum yield: f = 64 % (ref.: p- terphenyl ( f = 93 % in cyclohexane) [2]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.09 V. s10
11 2,5-Bis(3,5-dimethylphenyl)furan (2e) The synthesis was carried out according to the general procedure with 464 mg (2.00 mmol) of 3,5-dimethyliodobenzene (3e) (Alfa Aesar). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n- hexane as an eluent to give 60.0 mg (0.22 mmol, 22%) of the desired product as colorless crystals. R f : = 0.43 (n-hexane). Mp 147 C. 1 H NMR (DMSO-d 6, 600 MHz): = 2.50 (s, 12 H), 6.93 (s, 2 H), 6.99 (s, 2 H), 7.42 (s, 4 H). 13 C NMR (DMSO, 150 MHz): = 21.0 (CH), (CH), (CH), (CH), (C quat ), (C quat ), 152,7 (C quat ). GC-MS (m/z (%)): 276 (M +, 100), 233 (4), 143 ((C 11 H 11 ) +, 11), 128 (11), 115 (10), 105 ((C 8 H 9 ) +, 11), 77 (14). IR (KBr): = 2913 (m) cm -1, 1601 (m), 1466 (m), 1377 (w), 1312 (w), 1207 (w), 1028 (m), 941 (m), 891 (m), 845 (s), 791 (s), 698 (m), 675 (m). Anal. calcd for C 20 H 20 O (276.4): C 86.92, H 7.29; Found: C 86.73, H UV vis (CH 2 Cl 2 ): max ( ): 331 nm (28000 L mol -1 cm -1 ), 347 (18000). Fluorescence (CH 2 Cl 2 ): max : 362 nm. Stokes shift: Δ = 3800 cm -1. Quantum yield: f = 55 % (ref.: p- terphenyl ( f = 93 % in cyclohexane) [2]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.06 V. s11
12 2,5-Bis(3-methoxyphenyl)furan (2f) [12] The synthesis was carried out according to the general procedure with 468 mg (2.00 mmol) of m-methoxyiodobenzene (3f) (Sigma Aldrich). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n- hexane as an eluent to give 110 mg (0.39 mmol, 39%) of the desired product as beige solid. R f : = 0.08 (n-hexane). Mp 85 C (colorless oil [12]). 1 H NMR (DMSO-d 6, 600 MHz): = 3.83 (s, 6 H), 6.89 (ddd, 3 J = 8.1 Hz, 4 J = 2.4 Hz, 5 J = 1.2 Hz, 2 H), 7.10 (s, 2 H), (m, 4 H), 7.40 (td, 3 J = 7.8 Hz, 4 J = 1.2 Hz, 4 H). 13 C NMR (DMSO, 150 MHz): = 55.2 (CH), (CH), (CH), (CH), (CH), (CH), (C quat ), (C quat ), (C quat ). GC-MS (m/z (%)): 280 (M +, 100), 237 (23), 194 (16), 165 (13), 145 (9), 102 (21), 92 (17), 77 (22), 63 (16), 51 (9). IR (KBr): = 2959 (w) cm -1, 1611 (w), 1584 (m), 1485 (s), 1431 (m), 1279 (m), 1211 (s), 1169 (m), 1099 (w), 1038 (s), 864 (m), 796 (s), 777 (m), 692 (m), 681 (m). Anal. calcd for C 18 H 16 O 3 (280.3): C 77.12, H 5.75; Found: C 77.04, H UV vis (CH 2 Cl 2 ): max ( ): 331 nm (29000 L mol -1 cm -1 ), 347 (20000). Fluorescence (CH 2 Cl 2 ): max : 362 nm. Stokes shift: Δ = 4000 cm -1 ); Quantum yield: f = 95 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [2]). s12
13 2,5-Bis(3,4,5-trimethoxyphenyl)furan (2g) [13] The synthesis was carried out according to the general procedure with 588 mg (2.00 mmol) of 3,4,5-trimethoxyiodobenzene (3g). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with 5/1 n-hexane/thf as an eluent to give 108 mg (0.27 mmol, 27%) of the desired product as colorless solid. R f : = 0.18 (5/1 n-hexane/thf). Mp 139 C ( C [13]). 1 H NMR (DMSO-d 6, 600 MHz): = 3.70 (s, 6 H), 3.88 (s 12 H), 7.07 (s 2 H), 7.09 (s 4 H). 13 C NMR (DMSO, 150 MHz): = 56.0 (CH t ), 60.1 (CH), (CH), (CH), (C quat ), (C quat ), (C quat ), (C quat ). MS-EI (m/z (%)): 400 (M +, 4), 293 (13), 195 ((C 9 H 11 O 3 ) +, 3), 167 (19), 148 (100), 71 (23). IR (KBr): = 2951 (w) cm -1, 1586 (m), 1493 (m) 1464 (m), 1414 (m), 1341 (m), 1240 (m), 1184 (w), 1123 (s), 1088 (m), 1022 (m), 1007 (m), 997 (m), 968 (m), 831 (m), 789 (m), 762 (m), 691 (m). Anal. calcd for C 22 H 24 O 7 (400.4): C 66.59, H 6.04; Found: C 66.32, H UV vis (CH 2 Cl 2 ): max ( ): 340 nm (33000 L mol -1 cm -1 ), 365 (20000). Fluorescence (CH 2 Cl 2 ): max : 378 nm. Stokes shift: Δ = 3800 cm -1. Quantum yield: f = 80 % (ref.: p- terphenyl ( f = 93 % in cyclohexane) [2]). s13
14 2,5-Bis(2-methoxy-5-methylphenyl)furan (2h) [14] The synthesis was carried out according to the general procedure with 496 mg (2.00 mmol) of 2-iodo-1-methoxy-4-methylbenzene (3h). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 128 mg (0.42 mmol, 42%) of the desired product as yellow solid. R f : = 0.32 (n-hexane). Mp 118 C (110 C [14]). 1 H NMR (DMSO-d 6, 600 MHz): = 2.34 (s, 6 H), 3.89 (s 6 H), 7.00 (t, 3 J = 4.2 Hz, 4 H), 7.09 (dd, 3 J = 6.6 Hz, 4 J = 1.8 Hz, 2 H), 7.75 (ds, 4 J = 1.8 Hz, 2 H). 13 C NMR (DMSO, 150 MHz): = 20.3 (CH), 55.9 (CH), (CH), (CH), (C quat ), (CH), (CH), (C quat ), (C quat ), (C quat ). GC-MS (m/z (%)): 308 (M +, 100), 265 (42), 149 ((C 9 H 9 O 2 ) +, 23), 145 (45), 115 (40), 91 (32), 78 (45). IR (KBr): = 2926 (w) cm -1, 1609 (w), 1503 (s), 1462 (m), 1439 (m), 1273 (m), 1244 (s), 1179 (m), 1146 (m), 1028 (s), 885 (w), 795 (s), 739 (m). Anal. calcd for C 20 H 20 O 3 (308.4): C 77.90, H 6.54; Found: C 77.93, H UV vis (CH 2 Cl 2 ): max ( ): 347 nm (33000 L mol -1 cm -1 ), 364 (26000). Fluorescence (CH 2 Cl 2 ): max : 377 nm. Stokes shift: Δ = 3500 cm -1. Quantum yield: f = 47 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [2]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 0.95 V. s14
15 2,5-Bis(naphthalen-1-yl)furan (2i) [15] The synthesis was carried out according to the general procedure with 508 mg (2.00 mmol) of 1-iodonaphtalene (3i). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 191 mg (0.60 mmol, 60%) of the desired product as beige solid. R f : = 0.43 (n-hexane). Mp 76 C (yellow oil [15]). 1 H NMR (DMSO-d 6, 600 MHz): = 7.19 (s, 2 H), (m, 6 H), 7.94 (d, 3 J = 7.1 Hz, 2 H), 7.99 (d, 3 J = 8.2 Hz, 2 H), 8.00 (d, 3 J = 8.0 Hz, 2 H), 8.53 (d, 3 J = 8.4 Hz, 2 H). 13 C NMR (DMSO, 150 MHz): = (CH), (CH), (CH), (CH), (CH), (CH), (C quat ), (CH), (C quat ), (C quat ), (C quat ). GC-MS (m/z (%)): 320 (M +, 100), 289 (9), 165 ((C 13 H 9 ) +, 30), 127 ((C 10 H 7 ) +, 57), 77 (12).IR (KBr): = 1479 (w) cm -1, 1446 (w), 1155 (w), 1022 (m), 925 (w), 910 (w), 794 (m), 756 (s), 689 (s), 671 (m). Anal. calcd for C 24 H 16 O (320.4): C 89.97, H 5.03; Found: C 89.69, H UV vis (CH 2 Cl 2 ): max ( ): 347 nm (29000 L mol -1 cm -1 ). Fluorescence (CH 2 Cl 2 ): max : 424 nm. Stokes shift: Δ = 5300 cm -1. Quantum yield: f = 75 % (ref.: coumarin 1 ( f = 73 % in EtOH) [3]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.15 V. s15
16 2,5-Bis(naphthalen-2-yl)furan (2j) [15] The synthesis was carried out according to the general procedure with 508 mg (2.00 mmol) of 2-iodonapthalene (3j). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 96.0 mg (0.21 mmol, 21%) of the desired product as brown solid. R f : = 0.28 (n-hexane). Mp 201 C ( C [15]). 1 H NMR (CDCl 3, 600 MHz): = 6.84 (s, 2 H), 7.40 (t, 3 J = 7.2 Hz, 2 H), 7.44 (t, 3 J = 7.2, 2 H), 7.76 (d, 3 J = 7.9, 2 H), 7.81 (s, 4 H), 7.86 (d, 3 J = 8.0, 2 H). 13 C NMR (DMSO, 150 MHz): = (CH), (CH), (CH), (CH), (CH), (CH), (C quat ), (CH), (CH), (C quat ), (C quat ), (C quat ). GC-MS (m/z (%)): 320 (M +, 100), 289 (6), 165 ((C 13 H 9 ) +, 16), 127 ((C 10 H 7 ) +, 18), 77 (3). IR (KBr): = 2922 (w) cm -1, 1661 (w), 1624 (w), 1599 (w), 1501 (w), 1375 (w), 1260 (m), 1090 (m), 1024 (m), 1015 (m), 795 (s), 741 (s). HRMS calcd for C 24 H 16 O + : ; Found: UV vis (CH 2 Cl 2 ): max ( ): 358 nm (26000 L mol -1 cm -1 ), 377 (21000). Fluorescence (CH 2 Cl 2 ): max : 393 nm. Stokes shift: Δ = 3600 cm -1. Quantum yield: f = 100 % (ref.: coumarin 1 ( f = 73 % in EtOH) [3]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.20 V. s16
17 2,5-Bis(3-hydroxymethylphenyl)furan (2k) The synthesis was carried out according to the general procedure with 636 mg (2.00 mmol) of THP protected 3-iodobenzyl alcohol (3k). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 120 mg (0.43 mmol, 43%) of the desired product as beige solid. R f : = 0.29 (n-hexane). Mp 146 C. 1 H NMR (DMSO-d 6, 600 MHz): = 4.57 (d, 3 J = 6.0 Hz, 4 H), 5.30 (t, 3 J = 5.4 Hz, 2 H), 7.06 (s, 2 H), 7.27 (d, 3 J = 7.2 Hz, 2 H), 7.41 (t, 3 J = 6.0 Hz, 2 H), 7.68 (d, 3 J = 7.8 Hz, 2 H), 7.77 (s, 2 H). 13 C NMR (DMSO, 150 MHz): = 62.8 (CH 2 ), (CH), (CH), (CH), (CH), (CH), (C quat ), (C quat ), (C quat ). MS-EI (m/z (%)): 280 (M +, 100), 261 (5), 202 (6), 191 (5), 145 ((C 10 H 9 O) +, 11), 135 ((C 8 H 7 O 3 ) +, 7), 107 ((C 7 H 7 O) +, 4),89 (8), 77 (6). IR (KBr): = 3277 (m) cm -1, 2924 (w), 1601 (w), 1476 (w), 1452 (m), 1414 (m), 1294 (m), 1184 (m), 1045 (m), 1026 (s), 1003 (s), 941 (m), 897 (m), 901 (s), 775 (s), 694 (s), 613 (m). Anal. calcd for C 18 H 16 O 3 (280.3): C 77.12, H 5.75; Found: C 76.88, H UV vis (CH 2 Cl 2 ): max ( ): 329 nm (32000 L mol -1 cm -1 ), 345 (22000). Fluorescence (CH 2 Cl 2 ): max : 362 nm. Stokes shift: Δ = 3900 cm -1. Quantum yield: f = 80 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [3]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.16 V. s17
18 2,5-Bis(thiophen-2-yl)furan (2l) [16] The synthesis was carried out according to the general procedure with 420 mg (2.00 mmol) of 2-iodothiophene (3l). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 73.0 mg (0.31 mmol, 31 %) of the desired product as colorless solid. R f : 0.31 (n-hexane). Mp 78 C (81-82 C [16]). 1 H NMR (DMSO-d 6, 600 MHz): = 6.85 (s, 2 H), 7.13 (t, 3 J = 3.7 Hz, 2 H), 7.42 (d, 3 J = 3.6 Hz, 2 H), 7.55 (d, 3 J = 5.0 Hz, 2 H). 13 C NMR (DMSO, 150 MHz): = (CH), (CH), (CH), (CH), (C quat ), (C quat ). GC-MS (m/z (%)): 232 (M +, 100), 203 (29), 171 (31), 121 (M-C 5 H 3 OS) +, 26), 111 ((M-C 7 H 5 O) +, 34), 83 ((C 4 H 3 S) +, 12), 77 (17), 69 (17), 63 (13), 58 (16), 51 (11). IR (KBr): = 3105 (w) cm -1, 1796 (w), 1429 (w), 1260 (w), 1003 (s), 843 (m), 826 (m), 789 (s), 691 (s). Anal. calcd for C 12 H 8 OS 2 (232.3): C 62.04, H 3.47, S 27.60; Found: C 62.27, H 3.39, S UV vis (CH 2 Cl 2 ): max ( ): 353 nm (24000 L mol -1 cm -1 ), 371 (15000). Fluorescence (CH 2 Cl 2 ): max : 389 nm. Stokes shift: Δ = 3800 cm -1. Quantum yield: f = 42 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [2]). s18
19 2,5-Bis(thiophen-3-yl)furan (2m) [17] The synthesis was carried out according to the general procedure with 420 mg (2.00 mmol) of 3-iodothiophene (3m). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 45.0 mg (0.20 mmol, 20 %) of the desired product as colorless solid. R f : = 0.22 (n-hexane). Mp 131 C ( C [17]). 1 H NMR (DMSO-d 6, 600 MHz): = 6.82 (s, 2 H), 7.50 (dd, 5 J = 0.6 Hz, 3 J = 5.0 Hz, 2 H), (m, 2 H), 7.79 (dd, 5 J = 1.1 Hz, 4 J = 3.0 Hz, 2 H). 13 C NMR (DMSO, 150 MHz): = (C quat ), (C quat ), (C quat ), (C quat ), (CH), (CH). GC-MS (m/z (%)): 232 (M +, 100), 203 (20.6), 171 (13.9), 121 ((M-C 7 H 8 S + ) 20.9), 111 ((M-C 5 H 5 OS) +, 25.0), 83 ((M-C 5 H 3 S) +, 11.4). IR (KBr): = 3101 (w), 2920 (w), 1573 (w), 1483 (w) 1413 (w), 1269 (w), 1085 (w), 1018 (m), 848 (m), 769 (s), 684 (m). HRMS calcd for C 13 H 8 OS + 2 : ; Found: UV vis (CH 2 Cl 2 ): max ( ): 321 nm (23000 L mol -1 cm -1 ), 336 (15000). Fluorescence (CH 2 Cl 2 ): max : 351 nm. Stokes shift: Δ = 3900 cm -1. Quantum yield: f = 29 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [2]). s19
20 2,5-Bis(phenanthren-9-yl)furan (2n) The synthesis was carried out according to the general procedure with 608 mg (2.00 mmol) of 9-iodophenanthrene (3n). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with 80/1 n-hexane/thf as an eluent to give 215 mg (0.51 mmol, 51%) of the desired product as yellow solid. R f : = 0.30 (40/1 n-hexane/thf). Mp 157 C. 1 H NMR (DMSO-d 6 measured at 80 C (DMSO-d 6 Signal locked at 3.5 ppm), 600 MHz): = 7.21 (s, 2.H), 7.68 (dt, 3 J = 7.2 Hz, 4 J = 1.2 Hz, 2 H), (m, 6 H), 8.09 (d, 2 H), 8.27 (s, 2 H), 8.57 (dd, 3 J = 9, 4 J = 1.8 Hz, 2 H), 8.83 (d, 3 J = 7.8 Hz, 2 H), 8.92 (dd, 3 J = 9 Hz, 4 J = 1.8 Hz, 2 H). 13 C NMR (DMSO-d 6 measured at 80 C (DMSO-d6 Signal locked at 39.5 ppm), 150 MHz): = (CH), (CH), (CH), (C quat ), (CH), (CH), (CH), (CH), (CH), (CH), (C quat ), (CH), (C quat ), (C quat ), (C quat ), (C quat ). MS-EI (m/z (%)): 420 (M +, 100), 389 (12), 376 (11), 215 ((C 17 H 11 ) +, 22), 205 ((C 15 H 9 O) +, 14), 188 (22), 177 ((C 14 H 9 ) +, 21); IR (KBr): = 3053 (w) cm -1, 1940 (w), 1609 (w), 1493 (w), 1447 (m), 1425 (m), 1250 (m), 1140 (m), 897 (s), 764 (s), 743 (s), 717 (s). Anal. calcd for C 32 H 20 O (420.5): C 91.40, H 4.79; Found: C 91.18, H UV vis (CH 2 Cl 2 ): max ( ): 343 nm (23000 L mol -1 cm -1 ). Fluorescence (CH 2 Cl 2 ): max : 439 nm. Stokes shift: Δ = 6400 cm -1. Quantum yield: f = 69 % (ref.: coumarin 1 ( f = 73 % in EtOH) [3]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.24 V. s20
21 2,5-Bis(4-fluorophenyl)furan (2o) [12] The synthesis was carried out according to the general procedure with 444 mg (2.00 mmol) of p-fluoroiodobenzene (3o) (ABCR). The crude product was absorbed onto Celite and purified by column chromatography on silica gel with n-hexane as an eluent to give 63.0 mg (0.25 mmol, 25%) of the desired product as colorless crystals. R f : = 0.33 (n-hexane). Mp 146 C ( C [12]). 1 H NMR (DMSO-d 6, 600 MHz): = 7.05 (s, 2 H), 7.29 (t, 3 J = 6.0 Hz, 2 H), 7.86 (dt, 3 J = 5.4 Hz, 4 J = 3 Hz, 4 H). 13 C NMR (DMSO, 150 MHz): = (CH), (d, 2 J = 21.9 Hz, CH), (d, 3 J = 8.1 Hz, CH), (d, 4 J = 3 Hz, C quat ), (C quat ), (d, 1 J = Hz, C quat ). GC-MS (m/z (%)): 256 (M +, 100), 227 (13), 207 (5), 133 ((C 9 H 6 F) +, 22), 123 ((C 7 H 4 FO) +, 18), 95 ((C 6 H 4 F) +, 16). IR (KBr): = 2924 (w) cm -1, 1599 (m), 1487 (s), 1300 (m), 1229 (s), 1157 (m), 1103 (m), 1026 (m), 928 (m), 829 (s), 810 (m), 787 (m), 774 (s), 664 (m), 635 (m), 623 (s). Anal. calcd for C 16 H 10 F 2 O (256.3): C 74.99, H 3.93; Found.: C 74.82, H UV vis (CH 2 Cl 2 ): max ( ): 323 nm (21000 L mol -1 cm - 1 ), 338 (12000). Fluorescence (CH 2 Cl 2 ): max : 353 nm. Stokes shift: Δ = 3800 cm -1. Quantum yield: f = 76 % (ref.: p-terphenyl ( f = 93 % in cyclohexane) [2]). Cyclic voltammetry (CH 2 Cl 2 ): E 0/+1 1/2 = 1.24 V, reversible. s21
22 5. UV-absorption and fluorescence data of compounds 2a 2o E 0-0 was determined with the cross-section of the absorption and emission spectra ( ). 2,5-Diphenylfuran (2a) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). s22
23 2,5-Di-o-tolylfuran (2b) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). 2,5-Di-m-tolylfuran (2c) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). s23
24 2,5-Di-p-tolylfuran (2d) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). 2,5-Bis(3,5-dimethylphenyl)furan (2e) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). s24
25 2,5-Bis(3-methoxyphenyl)furan (2f) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). 2,5-Bis(3,4,5-trimethoxyphenyl)furan (2g) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). s25
26 2,5-Bis(2-methoxy-5-methylphenyl)furan (2h) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). 2,5-Di(naphthalen-1-yl)furan (2i) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). s26
27 2,5-Di(naphthalen-2-yl)furan (2j) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). 2,5-Bis(3-hydroxymethylphenyl)furan (2k) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). s27
28 2,5-Di(thiophen-2-yl)furan (2l) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). 2,5-Di(thiophen-3-yl)furan (2m) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). s28
29 2,5-Di(phenanthren-9-yl)furan (2n) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). 2,2,5-bis(4-fluorophenyl)furan (2o) Normalized UV vis and fluorescence spectra (recorded in dichloromethane at T = 20 C). s29
30 6. NMR spectra of compounds 2a 2o 2,5-Diphenylfuran (2a) 1 H NMR of 2a in DMSO-d 6 at T = 298 K (600 MHz) C NMR of 2a in DMSO-d 6 at T = 298 K (150 MHz). s30
31 DEPT-135 NMR of 2a in DMSO-d 6 at 298 K (150 MHz). s31
32 2,5-Di-o-tolylfuran (2b) 1 H NMR of 2b in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2b in DMSO-d 6 at T = 298 K (150 MHz). s32
33 DEPT-135 NMR of 2b in DMSO-d 6 at T = 298 K (150 MHz). s33
34 2,5-Di-m-tolylfuran (2c) 1 H NMR of 2c in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2c in DMSO-d 6 at T = 298 K (150 MHz). s34
35 DEPT-135 NMR of 2c in DMSO-d 6 at T = 298 K (150 MHz). s35
36 2,5-Di-p-tolylfuran (2d) 1 H NMR of 2d in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2d in DMSO-d 6 at T = 298 K (150 MHz). s36
37 DEPT-135 NMR of 2d in DMSO-d 6 at T = 298 K (150 MHz). s37
38 2,5-Bis(3,5-dimethylphenyl)furan (2e) 1 H NMR of 2e in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2e in DMSO-d 6 at T = 298 K (150 MHz). s38
39 DEPT-135 NMR of 2e in DMSO-d 6 at T = 298 K (150 MHz). s39
40 2,5-Bis(3-methoxyphenyl)furan (2f) 1 H NMR of 2f in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2f in DMSO-d 6 at T = 298 K (150 MHz). s40
41 DEPT-135 NMR of 2f in DMSO-d 6 at T = 298 K (150 MHz). s41
42 2,5-Bis(3,4,5-trimethoxyphenyl)furan (2g) 1 H NMR of 2g in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2g in DMSO-d 6 at T = 298 K (150 MHz). s42
43 DEPT-135 NMR of 2g in DMSO-d 6 at T = 298 K (150 MHz). s43
44 2,5-Bis(2-methoxy-5-methylphenyl)furan (2h) 1 H NMR of 2h in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2h in DMSO-d 6 at T = 298 K (150 MHz). s44
45 DEPT-135 NMR of 2h in DMSO-d 6 at T = 298 K (150 MHz). s45
46 2,5-Bis(naphthalen-1-yl)furan (2i) 1 H NMR of 2i in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2i in DMSO-d 6 at T = 298 K (150 MHz). s46
47 DEPT-135 NMR of 2i in DMSO-d 6 at T = 298 K (150 MHz). s47
48 2,5-Bis(naphthalen-2-yl)furan (2j) 1 H NMR of 2j in CDCl 3 at T = 298 K (600 MHz). 13 C NMR of 2j in CDCl 3 at T = 298 K (150 MHz). s48
49 DEPT-135 NMR of 2j in CDCl 3 at T = 298 K (150 MHz). s49
50 2,5-Bis(3-hydroxymethylphenyl)furan (2k) 1 H NMR of 2k in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2k in DMSO-d 6 at T = 298 K (150 MHz). s50
51 DEPT-135 NMR of 2k in DMSO-d 6 at T = 298 K (150 MHz). s51
52 2,5-Bis(thiophen-2-yl)furan (2l) 1 H NMR of 2l in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2l in DMSO-d 6 at T = 298 K (150 MHz). s52
53 DEPT-135 NMR of 2l in DMSO-d 6 at T = 298 K (150 MHz). s53
54 2,5-Bis(thiophen-3-yl)furan (2m) 1 H NMR of 2m in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2m in DMSO-d 6 at T = 298 K (150 MHz). s54
55 DEPT-135 NMR of 2m in DMSO-d 6 at T = 298 K (150 MHz). s55
56 2,5-Bis(phenanthren-9-yl)furan (2n) 1 H NMR of 2n in DMSO-d 6 at T = 378 K (600 MHz). 13 C NMR of 2n in DMSO-d 6 at T = 378 K (150 MHz). s56
57 DEPT-135 NMR of 2n in DMSO-d 6 at T = 378 K (150 MHz). s57
58 2,5-Bis(4-fluorophenyl)furan (2o) 1 H NMR of 2o in DMSO-d 6 at T = 298 K (600 MHz). 13 C NMR of 2o in DMSO-d 6 at T = 298 K (150 MHz). s58
59 DEPT-135 NMR of 2o in DMSO-d 6 at T = 298 K (150 MHz). s59
60 7. CV data of compounds 2a 2o The oxidation potentials were determined with ( ) ( ) ([FeCp 2 ]/[FeCp 2 ] + (E 0/+1 0 = 450 mv) [4]). The half-wave potential against NHE were calculated with ( ) ( ) (NHE = V) The HOMO energy of all compounds were calculated with the first oxidation potential (vs NHE) of the corresponding molecule. ( ( ) ) The summand 4.6 ev is the ferrocene HOMO energy value related to the vacuum level [18]. 2,5-Diphenylfuran (2a) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. s60
61 2,5-Di-o-tolylfuran (2b) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. 2,5-Di-m-tolylfuran (2c) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. s61
62 2,5-Di-p-tolylfuran (2d) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. 2,5-Bis(3,5-dimethylphenyl)furan (2e) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. s62
63 2,5-Bis(2-methoxy-5-methylphenyl)furan (2h) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. 2,5-Di(naphthalen-1-yl)furan (2i) 0.1 M Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. s63
64 2,5-Di(naphthalen-2-yl)furan (2j) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. 2,5-Bis(3-hydroxymethylphenyl)furan (2k) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. s64
65 2,5-Di(phenanthren-9-yl)furan (2n) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. 2,2,5-Bis(4-fluorophenyl)furan (2o) Recorded in dichloromethane, T = 293 K, = 100 mv/s, 0.1 M electrolyt: [Bu 4 N][PF 6 ], Pt working electrode, Pt counter electrode, Ag/AgCl (in KCl) reference electrode. s65
66 8. xyz-coordinates and dihedral angles of compounds 2a 2o The geometries of the furans were optimized in DFT calculations with the B3LYP [5] functional and the 6-311G(d,p) [6-9] basis set as implemented in the program package Gaussian09 [10]. The minima were confirmed by analytical frequency analysis. To find the global minima the DFT calculation started from the trans configuration with a dihedral angle of 90 (Fig. 1). Figure s1: Example of starting configuration. x,y,z-coordinates of 2,5-diphenylthiophene (2a) Dehedral Angle θ = 1 SCF Done: E(RB3LYP) = Hartrees A.U. after 8 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C C C C C C C O C C C C C C s66
67 H H H H H H H H H H H H s67
68 x,y,z-coordinates of 2,5-di-o-tolylfuran (2b) Dehedral Angle θ = 35 SCF Done: E(RB3LYP) = Hartrees A.U. after 14 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C C C C C O C C C C C C C C C C H H H H H H H H H H H H H H H H s68
69 x,y,z-coordinates of 2,5-di-m-tolylfuran (2c) Dehedral Angle θ = 0 SCF Done: E(RB3LYP) = Hartrees A.U. after 12 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C O C C C C C C C C C C C C C C H H H H H H H H H H H H H H H H s69
70 x,y,z-coordinates of 2,5-di-p-tolylfuran (2d) Dehedral Angle θ = 0 SCF Done: E(RB3LYP) = Hartrees A.U. after 6 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C O C C C C C C C C C C C C C C H H H H H H H H H H H H H H H H s70
71 x,y,z-coordinates of 2,5-bis(3,5-dimethylphenyl)furan (2e) Dehedral Angle θ = 0 SCF Done: E(RB3LYP) = Hartrees A.U. after 5 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C C C C C C C O C C C C C C C C C C H H H H H H H H H H H H H H H H s71
72 H H H H s72
73 x,y,z-coordinates of 2,5-bis(3-methoxyphenyl)furan (2f) Dehedral Angle θ = 0 SCF Done: E(RB3LYP) = Hartrees A.U. after 14 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C O C C C C C C C C C C C C O O C C H H H H H H H H H H H H H H H H s73
74 x,y,z-coordinates of 2,5-bis(3,4,5-trimethoxyphenyl)furan (2g) Dehedral Angle θ = 2 SCF Done: E(RB3LYP) = Hartrees A.U. after 5 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C C C C C C C O C C C C C C O C O C O C O C O C O C H H H H H H H s74
75 H H H H H H H H H H H H H H H H H s75
76 x,y,z-coordinates of 2,5-bis(2-methoxy-5-methylphenyl)furan (2h) Dehedral Angle θ = 38 SCF Done: E(RB3LYP) = Hartrees A.U. after 13 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C O C C C C C C C C C C C C C C O O C C H H H H H H H H H H H H H H s76
77 H H H H H H s77
78 x,y,z-coordinates of 2,5-bis(naphthalen-1-yl)furan (2i) Dehedral Angle θ = 42 SCF Done: E(RB3LYP) = Hartrees A.U. after 14 cycles Sum of electronic and zero-point Energies= Hartrees Sum of electronic and thermal Energies= Hartrees Sum of electronic and thermal Enthalpies= Hartrees Sum of electronic and thermal Free Energies= Hartrees C C C C O C C C C C C C C C C C C C C C C C C C C H H H H H H H H H H H H s78
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