Introduction of a new synthetic route about (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

With the rapid development of chemical substances, we look forward to future research findings about 246047-72-3

(1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, cas is 246047-72-3, it is a common heterocyclic compound, the ruthenium-catalysts compound, its synthesis route is as follows.,246047-72-3

To a solution of 13b (40.0 mg, 0.065 mmol) in anhydrous CH2Cl2 (6.0 ml) was added2nd generation Grubbs catalyst (50.3 mg, 0.059 mmol) and CuCl (I) (13.0 mg, 0.13mmol) under nitrogen at 30 C and stirred for 3 h. The reaction mixture was concentrated in vacuo, and the residue was purified by column chromatography onsilica gel (hexane / AcOEt = 2 / 1) to give 3b (55.5 mg, 78%).green crystals; mp 160-165 C (dec.); 1H NMR (270 MHz, CDCl3) delta 2.01-2.04 (m, 2H),2.22-2.31 (m, 2H), 2.43 (d, J = 14.8 Hz, 18H), 2.77-2.87 (m, 4H), 4.10-4.21 (m, 6H),6.51 (s, 1H), 7.08 (s, 5H), 16.43 (s, 1H); 19F NMR (466 MHz, CDCl3) delta -80.5 (3F),-114.4 (2F), -121.5 (2F), -121.8 (4F), -122.5 (2F), -123.3 (2F), -126.0 (2F); 13C NMR(68 MHz, CDCl3) delta 19.2, 21.0, 22.5, 23.5, 51.7, 69.5, 77.5, 118.9, 124.1, 128.9, 129.5,133.2, 136.3, 138.7, 143.7, 148.5, 210.7, 291.4; IR (FT) 3905, 3857, 3816, 3743, 3700,3642, 3616, 3569, 3013, 2945, 2913, 2856, 2363, 2331, 1738, 1691, 1596, 1555, 1476,1455, 1413, 1245, 1203, 1140, 1108, 1035, 993, 915, 857, 814, 730 cm-1; HRMS (FAB)m/z [M+H]+ calcd for C41H40Cl2F17N2ORu 1072.1290, found 1072.1320.

With the rapid development of chemical substances, we look forward to future research findings about 246047-72-3

Reference£º
Article; Kobayashi, Yuki; Suzumura, Naoki; Tsuchiya, Yuki; Goto, Machiko; Sugiyama, Yuya; Shioiri, Takayuki; Matsugi, Masato; Synthesis; vol. 49; 8; (2017); p. 1796 – 1807;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Some tips on 15529-49-4

15529-49-4, The synthetic route of 15529-49-4 has been constantly updated, and we look forward to future research findings.

15529-49-4, Dichlorotris(triphenylphosphino)ruthenium (II) is a ruthenium-catalysts compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

To a solution of ONS-LH (486mg, 2.0mmol) in THF (20mL) was added [Ru(PPh3)3Cl2] (868mg, 2.0mmol), which was then stirred under N2 for 15min. Triethylamine (Et3N) (202mg, 2.0mmol) was introduced, and the reaction mixture was stirred overnight at room temperature, during which the color of solution changed from brown to dark red brown. After removal of solvents in vacuo, CH2Cl2 (20mL) was added and the solution was filtered. The filtrate was concentrated and the residue was washed with Et2O (5mL¡Á2) and hexane (5mL¡Á2) to give the desired product. Recrystallization from MeOH/ Et2O (1:3) afforded dark red block crystals of 1¡¤0.5CH3OH¡¤2.75H2O suitable for X-ray diffraction in five days. Yield: 1.19g, 63% (based on Ru). IR (KBr disc, cm-1): 1597 (nuC=N), 1311 (nuC-O), 739 (nuC-S), 1432, 1087 and 691 (nuPPh3); 31P NMR (CDCl3, 162MHz): delta 16.4 (s, PPh3), 14.7 (s, PPh3) ppm. 1H NMR (CDCl3, 400MHz): delta 8.81 (s, 1H, CH=N), 7.98-7.31 (m, 4H, Ar-H), 7.23-7.06 (m, 4H, Ar-H), 6.75-7.01 (m, 30H, PPh3), 2.39 (s, 3H, SCH3) ppm. MS (FAB): m/z 903 [M+], 868 [M+-Cl], 641 [M+-PPh3], 379 [M+-2PPh3], 344 [Ru(ONS-L)]+. Anal. Calc. for C50H42NOP2ClSRu¡¤0.5(CH4O)¡¤2.75(H2O) (%): C, 64.74; H, 4.98; N, 1.48. Found: C, 64.67; H, 5.03; N, 1.43

15529-49-4, The synthetic route of 15529-49-4 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Wang, Chang-Jiu; Lin, Hui; Chen, Xin; Jia, Ai-Quan; Zhang, Qian-Feng; Inorganica Chimica Acta; vol. 467; (2017); p. 198 – 203;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

New learning discoveries about 246047-72-3

246047-72-3 (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium 11147261, aruthenium-catalysts compound, is more and more widely used in various.

246047-72-3, (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium is a ruthenium-catalysts compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

246047-72-3, Example 52 Synthesis of Ru complex 6a To a 50 mL two-necked round bottom flask, after filling with Ar atmosphere, were added ligand 5a (l .Ommol) and CuCl (3.0mmol, 3eq) and 30 mL dry DCM, followed by refilling with Ar three times and protected with Ar balloon in close system. Ru complex lb (l.Ommol) was added under Ar protection, and the mixture was stirred for 0.5 hr at room temperature. After the reaction was complete, the solution was filtered and the filtrate was concentrated and slurred with silica gel. The crude was obtained by silica gel column chromatography and washed with methanol or pentane-DCM to obtain 453mg of yellow-green solid product 6a, yield: 79%. Ru complex (6a) 1HNMR (400 MHz, CDC13): delta 18.53 (s, 1H, Ru=CH), 8.59 (s, 1H), 7.28-6.49 (m, 11H), 4.160 (s, 4H, NCH2CH2N), 2.50 (s, 12H), 2.42 (s, 6H).; Example 59 Synthesis of Ru complex 6h The synthetic procedure is the same as in Example 52 in 1.0 mmol scale. 106 mg of yellow-green solid product 6h was obtained (37% yield). Ru complex (6h) 1HNMR (400 MHz, CDC13): delta 16.52 (s, 1H, Ru=CH), 8.43 (s,1H, N=CH), 8.10 (s, 1H), 7.46-7.22 (m, 2H), 7.73-6.96 (m, 8H), 4.19 (s, 4H, NCH2CH2N), 3.95 (s, 3H), 3.87 (s, 3H), 2.49 (s, 12H), 2.48 (s, 6H).

246047-72-3 (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium 11147261, aruthenium-catalysts compound, is more and more widely used in various.

Reference£º
Patent; ZANNAN SCITECH CO., LTD.; ZHAN, James Zheng-Yun; WO2011/79439; (2011); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Some tips on 15529-49-4

15529-49-4, The synthetic route of 15529-49-4 has been constantly updated, and we look forward to future research findings.

15529-49-4, Dichlorotris(triphenylphosphino)ruthenium (II) is a ruthenium-catalysts compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A mixture of [RuCl2(PPh3)3] (50 mg, 0.052 mmol) and bipy (10mg, 0.06 mmol) were charged in a two necked round bottomed flask and kept under vacuum for 15 min. 20 mL of dry acetone was then added and the brown mixture was stirred under argon atmosphere for approximately 30 min. A light yellowish-brown solid was precipitated that was filtered off, washed with diethylether (2 5 mL) and subsequently dried in vacuo. Yield: 90 %(40 mg). UV-Vis (e, Mu1 cm1): kmax (CH2Cl2) = 490 (5370), 350(9640).

15529-49-4, The synthetic route of 15529-49-4 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Zacharopoulos, Nikolaos; Kolovou, Evgenia; Peppas, Anastasios; Koukoulakis, Konstantinos; Bakeas, Evangelos; Schnakenburg, Gregor; Philippopoulos, Athanassios I.; Polyhedron; vol. 154; (2018); p. 27 – 38;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Introduction of a new synthetic route about Dichlorotris(triphenylphosphino)ruthenium (II)

With the rapid development of chemical substances, we look forward to future research findings about 15529-49-4

Dichlorotris(triphenylphosphino)ruthenium (II), cas is 15529-49-4, it is a common heterocyclic compound, the ruthenium-catalysts compound, its synthesis route is as follows.,15529-49-4

General procedure: Diphosphine ligand (2.0 mmol) was dissolved in 10 mL of dichloromethane and the solution was added dropwise to a stirred solution of RuCl2(PPh3)3 (1.0 mmol) in 10 mL of dichloromethane. The reaction mixture was stirred approximately for 50 min at room temperature. The brown solution was filtered to remove the insoluble impurities. The solvent was reduced by a vacuum and the product was then precipitated by adding n-hexane. The yellow solid was filtered and washed three times with 20 mL of diethyl ether.

With the rapid development of chemical substances, we look forward to future research findings about 15529-49-4

Reference£º
Article; Al-Noaimi, Mousa; Warad, Ismail; Abdel-Rahman, Obadah S.; Awwadi, Firas F.; Haddad, Salim F.; Hadda, Taibi B.; Polyhedron; vol. 62; (2013); p. 110 – 119;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

New learning discoveries about 15529-49-4

15529-49-4, 15529-49-4 Dichlorotris(triphenylphosphino)ruthenium (II) 11007548, aruthenium-catalysts compound, is more and more widely used in various.

15529-49-4, Dichlorotris(triphenylphosphino)ruthenium (II) is a ruthenium-catalysts compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

c) Preparation of the Complex Dichloro bis[3-(Diphenylphosphino)-1-propylamine]Ruthenium; ([RuCl2(L-2)2]). Under argon, a round-bottomed Schlenck flask, equipped with a magnetic stirring bar, was charged with RuCl2(PPh3)3 (1.028 g, 1.07 mmol) and with a solution of 3-(diphenylphosphino)-1-propylamine (566.8 mg, 2.33 mmol) in toluene (5 mL). More toluene (5 mL) was added to rinse. Then the dark-brown solution was heated in an oil bath at 100 C. for 16 h. The resulting brick-orange suspension was cooled to room temperature, and added to pentane (50 mL) with stirring. The yellow solid was collected by filtration, washed with pentane (2¡Á3 mL) and dried in vacuo to provide the desired complex (672.6 mg, 1.02 mmol, 95%) as a yellow-mustard solid. 31P{1H}-NMR analysis showed the presence of two species. 1H-NMR (CD2Cl2): delta (A) 7.19 (t, J=7.2 Hz, 4H), 7.14 (m, 8H), 7.05 (t, J=7.2 Hz, 8H), 3.28 (brs, 4H), 3.02 (brs, 4H), 2.66 (m, 4H), 2.0 (m, 4H). 13C-NMR (CD2Cl2): delta (A) 138.4 (t, J=19.2 Hz, Carom), 134.2 (t, J=4.8 Hz, CHarom), 129.0 (CHarom), 127.5 (t, J=4.8 Hz, CHarom), 41.3 (CH2), 26.9 (t, J=13.6 Hz, CH2), 24.7 (CH2). 31P{1H}-NMR (CD2Cl2): A (82%) delta=33.5 ppm (s), B (18%) delta=49.8 ppm (s).

15529-49-4, 15529-49-4 Dichlorotris(triphenylphosphino)ruthenium (II) 11007548, aruthenium-catalysts compound, is more and more widely used in various.

Reference£º
Patent; SAUDAN, Lionel; Dupau, Philippe; Riedhauser, Jean-Jacques; Wyss, Patrick; US2008/71121; (2008); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Introduction of a new synthetic route about 246047-72-3

With the rapid development of chemical substances, we look forward to future research findings about 246047-72-3

(1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, cas is 246047-72-3, it is a common heterocyclic compound, the ruthenium-catalysts compound, its synthesis route is as follows.,246047-72-3

To a solution of 1-isopropoxy-4-(perfluorodecyl)-2-vinylbenzene (35.5mg, 0.052mmol) in dry CH2Cl2 (4 mL) was added Grubbs 2nd generation (48.75 mg, 0.057 mmol) and CuCl (I) (8.2 mg, 0.083 mmol) under N2 at 35C and stirred for 3 h. The reaction mixture was concentrated in vacuo, and the residue was purified by column chromatography on silica gel (hexane / CH2Cl2 = 1 / 1) to give 1a (39.5mg, 65%).

With the rapid development of chemical substances, we look forward to future research findings about 246047-72-3

Reference£º
Article; Kobayashi, Yuki; Inukai, Sae; Kondo, Natsuki; Watanabe, Tomoko; Sugiyama, Yuya; Hamamoto, Hiromi; Shioiri, Takayuki; Matsugi, Masato; Tetrahedron Letters; vol. 56; 11; (2015); p. 1363 – 1366;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Introduction of a new synthetic route about 15529-49-4

With the rapid development of chemical substances, we look forward to future research findings about 15529-49-4

Dichlorotris(triphenylphosphino)ruthenium (II), cas is 15529-49-4, it is a common heterocyclic compound, the ruthenium-catalysts compound, its synthesis route is as follows.,15529-49-4

General procedure: A methanol (10ml) solution containing the appropriate N-S pro-ligand and triethylamine was refluxed under argon for 15min and then the complex [RuCl2(PPh3)3] was added. The resulting brown suspension was refluxed for 3h, to afford a yellow suspension. After cooling, the yellow solid was collected by filtration, washed with methanol (3¡Á5ml), and dried under reduced pressure. 2.6.1 [Ru(mctz)2(PPh3)2] (1) Hmctz (0.019 g – 1.8 * 10-4 mol); NEt3 (26 mul – 1.8 * 10-4 mol), and [RuCl2(PPh3)3] (0.085 g – 8.9 * 10-5 mol). Yield: 50 mg – 65.8%. 31P{1H} NMR (81 MHz, CDCl3) 53.5 ppm (s). 1H NMR (200 MHz, CDCl3), delta/ppm: 7.4-7.0 (m, 30H Ph – PPh3); 3.4-2.5 (m (br), 8HCH2-mctz-). Anal. exp. (calc. for C42H38N2P2RuS4) C, 58.0 (58.5); H, 4.4 (4.4); N, 3.2 (3.2); S, 14.6 (14.9). Suitable single crystals were obtained by slow evaporation of a dichloromethane solution.

With the rapid development of chemical substances, we look forward to future research findings about 15529-49-4

Reference£º
Article; Appelt, Patricia; Fagundes, Francisco D.; Facchin, Gianella; Gabriela Kramer; Back, Davi F.; Cunha, Mario A.A.; Sandrino, Bianca; Wohnrath, Karen; De Araujo, Marcio P.; Inorganica Chimica Acta; vol. 436; (2015); p. 152 – 158;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Introduction of a new synthetic route about 15529-49-4

With the rapid development of chemical substances, we look forward to future research findings about 15529-49-4

Dichlorotris(triphenylphosphino)ruthenium (II), cas is 15529-49-4, it is a common heterocyclic compound, the ruthenium-catalysts compound, its synthesis route is as follows.,15529-49-4

To a solution of [Ru(PPh3)3Cl2] (868?mg, 2.0?mmol) in THF (10?mL) was added a solution of N,O-LH-NO2 (972?mg, 2.0?mmol) and Et3N (404?mg, 4.0?mmol) in EtOH (5?mL), and then the mixture was heated at 90?C with stirring overnight, during which there was a color change from brown to green. After removal of solvents in vacuo, the residue was extracted with CH2Cl2 (5?mL?*?2) and the solution was filtered. The clearly green filtrate was layered with Et2O (20?mL) at room temperature, and dark green block-shaped crystals of trans-[RuCl(PPh3)(kappa2-N,O-L-NO2)2]¡¤Et2O (2) were obtained in three days. Yield: 1356?mg, 71% (based on Ru).

With the rapid development of chemical substances, we look forward to future research findings about 15529-49-4

Reference£º
Article; Tang, Li-Hua; Wu, Fule; Lin, Hui; Jia, Ai-Quan; Zhang, Qian-Feng; Inorganica Chimica Acta; vol. 477; (2018); p. 212 – 218;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Introduction of a new synthetic route about 246047-72-3

With the rapid development of chemical substances, we look forward to future research findings about 246047-72-3

(1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, cas is 246047-72-3, it is a common heterocyclic compound, the ruthenium-catalysts compound, its synthesis route is as follows.,246047-72-3

To a solution of 6b (31.0 mg, 0.048 mmol) in anhydrous CH2Cl2 (5.0 ml) was added 2ndgeneration Grubbs catalyst (37.0 mg, 0.052 mmol) and CuCl (I) (9.6 mg, 0.097 mmol)under nitrogen at 30 C and stirred for 1 h. The reaction mixture was concentrated invacuo, and the residue was purified by column chromatography on silica gel (hexane /CH2Cl2 = 1 / 1) to give 2f (27.0 mg, 50%).Green crystals; mp 125-127 C (dec.); 1H NMR (270 MHz, CDCl3) delta 1.21 (d, J = 6.4Hz, 6H), 1.27 (d, J = 5.6 Hz, 6H), 2.37 (s, 6H), 2.47 (bs, 12H), 4.19 (s, 4H), 4.51-4.45(m, 1H), 5.89-5.80 (m, 1H), 6.70 (d, J = 1.3 Hz, 1H), 7.06 (s, 4H), 7.18 (d, J = 1.6 Hz,1H), 16.31 (s, 1H); 19F NMR (466 MHz, CDCl3) delta -80.5 (3F), -110.0 (2F), -121.3 (4F),-121.7 (4F), -122.5 (2F), -125.9 (2F); 13C NMR (68 MHz, CDCl3) delta 21.5, 21.9, 22.5,51.3, 75.7, 76.0, 113.7, 114.5, 116.6, 123.5, 125.5, 126.6, 127.5, 129.4, 139.0, 143.5,147.4, 151.2, 209.8, 296.5; IR (FT) 3854, 3738, 3649, 2978, 2931, 2361, 2342, 1481,1199, 1107, 1072, 910, 729 cm-1; HRMS (FAB) m/z [M+H]+ calcd forC42H45Cl2F17N2O2Ru: 1104.1630; found: 1104.1637.

With the rapid development of chemical substances, we look forward to future research findings about 246047-72-3

Reference£º
Article; Kobayashi, Yuki; Suzumura, Naoki; Tsuchiya, Yuki; Goto, Machiko; Sugiyama, Yuya; Shioiri, Takayuki; Matsugi, Masato; Synthesis; vol. 49; 8; (2017); p. 1796 – 1807;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI