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Synthesis, Structural Characterization, Catalytic Activity on Suzuki-Miyaura and Mizoroki-Heck Coupling Reaction of Dichloro[1-(2-metil-2-propenil)-3-(3,4,5- trimethoxybenzyl) benzimidazole-2-ylidene] pyridine palladium(II) Complex

Yıl 2018, Cilt: 22 Sayı: Özel, 105 - 109, 05.10.2018

Öz

N-heterocyclic carbene-metal complexes exhibit high activity as catalysts. Synthesis of new catalysts and their use in organic synthesis reactions is one of the most important work areas of coordination chemistry. In this study, with the goal of achieving highly efficient palladium catalyzed cross-coupling reactions under mild reaction conditions, 1-(2-metil-2-propenil-3-(3,4,5-
trimethoxybenzyl)benzimidazoliumchloride salt (1) and its Pd(II)-N-heterocyclic carbene complex (2) were synthesized. Structures of obtained both compounds characterized by elemental analysis, FT-IR, 1H NMR and 13C NMR spectroscopies. Afterward, Pd(II)-NHC (2) complex was investigated catalytic activities on SuzukiMiyaura and Mizoroki-Heck coupling reactions. It was observed that synthesized dichloro[1-(2-metil-2-propenil)-3-(3,4,5-trimethoxybenzyl)benzimidazole-2- ylidene]pyridine palladium(II) complex exhibited quite high activity on SuzukiMiyaura coupling reaction at water/isopropyl alcohol mixture

Kaynakça

  • [1] Díez-González, S., Marion, N., Nolan, S. P. 2009. N-heterocyclic carbenes in late transition metal catalysis. Chemical Reviews, 109(8), 3612-3676.
  • [2] Irikura, K., Goddard III K, W. A., Beauchamp, J. L. 1992. Singlet-triplet gaps in substituted carbenes CXY (X, Y= H, fluoro, chloro, bromo, iodo, silyl). Journal of the American Chemical Society, 114(1), 48-51.
  • [3] Feller, D., Borden, W. T., Davidson, E. R. 1980. Dependence of the singlet-triplet splitting in heterosubstituted carbenes on the heteroatom electronegativity and conformation. Chemical Physics Letters, 71(1), 22-26.
  • [4] Arduengo III, A. J., Harlow, R. L., Kline, M. 1991. A stable crystalline carbene [Erratum to document cited in CA114 (7): 62009r]. Journal of the American Chemical Society, 113(7), 2801-2801.
  • [5] Wanzlick, H. W., Schönherr, H. J. 1968. Direct synthesis of a mercury salt‐carbene complex. Angewandte Chemie International Edition, 7(2), 141-142.
  • [6] Öfele, K. 1968. 1, 3-Dimethyl-4-imidazolinyliden -(2)-pentacarbonylchrom ein neuer Übergangs metall-carben-komplex. Journal of Organometal lic Chemistry, 12(3), P42-P43.
  • [7] Kuhl, S., Schneider, R., Fort, Y. 2003. Transfer hydrogenation of imines catalyzed by a nickel (0)/NHC complex. Organometallics, 22(21), 4184-4186.
  • [8] Bortenschlager, M., Schütz, J., von Preysing, D., Nuyken, O., Herrmann, W. A., Weberskirch, R. 2005. Rhodium–NHC-complexes as potent catalysts in the hydroformylation of 1-octene. Journal of organometallic chemistry, 690(24), 6233-6237.
  • [9] Boubakri, L., Yasar, S., Dorcet, V., Roisnel, T., Bruneau, C., Hamdi, N., Ozdemir, I. 2017. Synthesis and catalytic applications of palladium N-heterocyclic carbene complexes as efficient pre-catalysts for Suzuki–Miyaura and Sonogashira coupling reactions. New Journal of Chemistry, 41(12), 5105-5113.
  • [10] Rouen, M., Queval, P., Falivene, L., Allard, J., Toupet, L., Crévisy, C., Mauduit, M. 2014. Cationic Bis‐N‐Heterocyclic Carbene (NHC) Ruthenium Complex: Structure and Application as Latent Catalyst in Olefin Metathesis. Chemistry-A European Journal, 20(42), 13716-13721.
  • [11] Berthon-Gelloz, G., Buisine, O., Brière, J. F., Michaud, G., Stérin, S., Mignani, G., Markó, I. E. 2005. Synthetic and structural studies of NHC–Pt (dvtms) complexes and their application as alkene hydrosilylation catalysts (NHC= N-heterocyclic carbene, dvtms= divinyltetramethylsiloxane). Journal of Organometallic Chemistry, 690(24), 6156-6168.
  • [12] Lazaro, G., Iglesias, M., Fernández‐Alvarez, F. J., Miguel, S., Pablo, J., Pérez‐Torrente, J. J., Oro, L. A. 2013. Synthesis of poly (silyl ether) s by Rhodium (I)–NHC catalyzed hydrosilylation: Homogeneous versus heterogeneous catalysis. ChemCatChem, 5(5), 1133-1141.
  • [13] Kantchev, E.A.B., Brian, C.J.O., Organ, M.G. 2006. Pd-N-heterocyclic carbene (NHC) catalysts for cross-coupling reactions. Aldrichimica Acta 39, 97–111.
  • [14] Sharif, S., Rucker, R. P., Chandrasoma, N., Mitchell, D., Rodriguez, M. J., Froese, R. D., Organ, M. G. 2015. Selective Monoarylation of Primary Amines Using the Pd‐PEPPSI‐IPentCl Precatalyst. Angewandte Chemie International Edition, 54(33), 9507-9511.
  • [15] Suzuki, A. 1999. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles. Journal of Organometallic Chemistry, 576(1), 147-168.
  • [16] Miyaura, N., Yamada, K., Suzuki, A. 1979. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Letters, 20(36), 3437-3440.
  • [17] Han, F. S. 2013. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts. Chemical Society Reviews, 42(12), 5270-5298.
  • [18] Bringmann, G., Gulder, T., Gulder, T. A., Breuning, M. 2010. Atroposelective total synthesis of axially chiral biaryl natural products. Chemical reviews, 111(2), 563-639.
  • [19] Alberico, D., Scott, M. E., Lautens, M. 2007. Aryl− aryl bond formation by transition-metal-catalyzed direct arylation. Chemical reviews, 107(1), 174-238.
  • [20] Narayan, S., Muldoon, J., Finn, M. G., Fokin, V. V., Kolb, H. C., Sharpless, K. B. 2005. “On water”: Unique reactivity of organic compounds in aqueous suspension. Angewandte Chemie International Edition, 44(21), 3275-3279.
  • [21] Butler, R. N., Coyne, A. G. 2010. Water: Nature’s Reaction Enforcer Comparative Effects for Organic Synthesis “In-Water” and “On-Water”. Chemical reviews, 110(10), 6302-6337
  • [22] Organ, M. G., Avola, S., Dubovyk, I., Hadei, N., Kantchev, E. A. B., O'Brien, C. J., Valente, C. 2006. A User‐Friendly, All‐Purpose Pd–NHC (NHC= N‐Heterocyclic Carbene) Precatalyst for the Negishi Reaction: A Step Towards a Universal Cross‐Coupling Catalyst. Chemistry-A European Journal, 12(18), 4749-4755.
  • [23] O'Brien, C. J., Kantchev, E. A. B., Valente, C., Hadei, N., Chass, G. A., Lough, A., Organ, M. G. 2006. Easily Prepared Air‐and Moisture‐Stable Pd–NHC (NHC= N‐Heterocyclic Carbene) Complexes: A Reliable, User‐Friendly, Highly Active Palladium Precatalyst for the Suzuki–Miyaura Reaction. Chemistry-a European Journal, 12(18), 4743-4748.
  • [24] Doǧan, Ö., Demir, S., Özdemir, İ., Cetinkaya, B. 2011. Palladium (II) NHC complexes containing benzimidazole ligand as a catalyst for C-N bond formation. Applied Organometallic Chemistry, 25(3), 163-167.

Dikloro [1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil) benzimidazol-2-iliden] piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi

Yıl 2018, Cilt: 22 Sayı: Özel, 105 - 109, 05.10.2018

Öz

N-heterosiklik karben-metal kompleksleri katalizör olarak yüksek aktivite göstermektedirler. Yeni katalizörlerin sentezlenmesi ve organik sentez tepkimelerinde kullanılması koordinasyon kimyasının en önemli çalışma alanlarından biridir. Bu çalışmada, ılımlı tepkime koşulları altında, yüksek verimli paladyum katalizli eşleşme tepkimelerini gerçekleştirmek amacıyla, 1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil)benzimidazolyum klorür tuzu (1)  ve bu yeni tuzdan Pd(II)-N-heterosiklik karben kompleksi (NHC) (2) sentezlendi. Elde edilen her iki bileşiğin yapısı elementel analiz, FT-IR, 1H NMR ve 13C NMR spektroskopileri ile karakterize edildi. Daha sonra Pd(II)-NHC (2) kompleksinin Suzuki-Miyaura ve Mizoroki-Heck eşleşme tepkimelerindeki katalitik aktivitesi incelendi. Sentezlenen dikloro[1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil) benzimidazol-2-iliden] piridin paladyum(II) kompleksinin Suzuki-Miyaura eşleşme tepkimesi için su-izopropil alkol karışımında oldukça yüksek aktivite gösterdiği gözlendi.

Kaynakça

  • [1] Díez-González, S., Marion, N., Nolan, S. P. 2009. N-heterocyclic carbenes in late transition metal catalysis. Chemical Reviews, 109(8), 3612-3676.
  • [2] Irikura, K., Goddard III K, W. A., Beauchamp, J. L. 1992. Singlet-triplet gaps in substituted carbenes CXY (X, Y= H, fluoro, chloro, bromo, iodo, silyl). Journal of the American Chemical Society, 114(1), 48-51.
  • [3] Feller, D., Borden, W. T., Davidson, E. R. 1980. Dependence of the singlet-triplet splitting in heterosubstituted carbenes on the heteroatom electronegativity and conformation. Chemical Physics Letters, 71(1), 22-26.
  • [4] Arduengo III, A. J., Harlow, R. L., Kline, M. 1991. A stable crystalline carbene [Erratum to document cited in CA114 (7): 62009r]. Journal of the American Chemical Society, 113(7), 2801-2801.
  • [5] Wanzlick, H. W., Schönherr, H. J. 1968. Direct synthesis of a mercury salt‐carbene complex. Angewandte Chemie International Edition, 7(2), 141-142.
  • [6] Öfele, K. 1968. 1, 3-Dimethyl-4-imidazolinyliden -(2)-pentacarbonylchrom ein neuer Übergangs metall-carben-komplex. Journal of Organometal lic Chemistry, 12(3), P42-P43.
  • [7] Kuhl, S., Schneider, R., Fort, Y. 2003. Transfer hydrogenation of imines catalyzed by a nickel (0)/NHC complex. Organometallics, 22(21), 4184-4186.
  • [8] Bortenschlager, M., Schütz, J., von Preysing, D., Nuyken, O., Herrmann, W. A., Weberskirch, R. 2005. Rhodium–NHC-complexes as potent catalysts in the hydroformylation of 1-octene. Journal of organometallic chemistry, 690(24), 6233-6237.
  • [9] Boubakri, L., Yasar, S., Dorcet, V., Roisnel, T., Bruneau, C., Hamdi, N., Ozdemir, I. 2017. Synthesis and catalytic applications of palladium N-heterocyclic carbene complexes as efficient pre-catalysts for Suzuki–Miyaura and Sonogashira coupling reactions. New Journal of Chemistry, 41(12), 5105-5113.
  • [10] Rouen, M., Queval, P., Falivene, L., Allard, J., Toupet, L., Crévisy, C., Mauduit, M. 2014. Cationic Bis‐N‐Heterocyclic Carbene (NHC) Ruthenium Complex: Structure and Application as Latent Catalyst in Olefin Metathesis. Chemistry-A European Journal, 20(42), 13716-13721.
  • [11] Berthon-Gelloz, G., Buisine, O., Brière, J. F., Michaud, G., Stérin, S., Mignani, G., Markó, I. E. 2005. Synthetic and structural studies of NHC–Pt (dvtms) complexes and their application as alkene hydrosilylation catalysts (NHC= N-heterocyclic carbene, dvtms= divinyltetramethylsiloxane). Journal of Organometallic Chemistry, 690(24), 6156-6168.
  • [12] Lazaro, G., Iglesias, M., Fernández‐Alvarez, F. J., Miguel, S., Pablo, J., Pérez‐Torrente, J. J., Oro, L. A. 2013. Synthesis of poly (silyl ether) s by Rhodium (I)–NHC catalyzed hydrosilylation: Homogeneous versus heterogeneous catalysis. ChemCatChem, 5(5), 1133-1141.
  • [13] Kantchev, E.A.B., Brian, C.J.O., Organ, M.G. 2006. Pd-N-heterocyclic carbene (NHC) catalysts for cross-coupling reactions. Aldrichimica Acta 39, 97–111.
  • [14] Sharif, S., Rucker, R. P., Chandrasoma, N., Mitchell, D., Rodriguez, M. J., Froese, R. D., Organ, M. G. 2015. Selective Monoarylation of Primary Amines Using the Pd‐PEPPSI‐IPentCl Precatalyst. Angewandte Chemie International Edition, 54(33), 9507-9511.
  • [15] Suzuki, A. 1999. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles. Journal of Organometallic Chemistry, 576(1), 147-168.
  • [16] Miyaura, N., Yamada, K., Suzuki, A. 1979. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Letters, 20(36), 3437-3440.
  • [17] Han, F. S. 2013. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts. Chemical Society Reviews, 42(12), 5270-5298.
  • [18] Bringmann, G., Gulder, T., Gulder, T. A., Breuning, M. 2010. Atroposelective total synthesis of axially chiral biaryl natural products. Chemical reviews, 111(2), 563-639.
  • [19] Alberico, D., Scott, M. E., Lautens, M. 2007. Aryl− aryl bond formation by transition-metal-catalyzed direct arylation. Chemical reviews, 107(1), 174-238.
  • [20] Narayan, S., Muldoon, J., Finn, M. G., Fokin, V. V., Kolb, H. C., Sharpless, K. B. 2005. “On water”: Unique reactivity of organic compounds in aqueous suspension. Angewandte Chemie International Edition, 44(21), 3275-3279.
  • [21] Butler, R. N., Coyne, A. G. 2010. Water: Nature’s Reaction Enforcer Comparative Effects for Organic Synthesis “In-Water” and “On-Water”. Chemical reviews, 110(10), 6302-6337
  • [22] Organ, M. G., Avola, S., Dubovyk, I., Hadei, N., Kantchev, E. A. B., O'Brien, C. J., Valente, C. 2006. A User‐Friendly, All‐Purpose Pd–NHC (NHC= N‐Heterocyclic Carbene) Precatalyst for the Negishi Reaction: A Step Towards a Universal Cross‐Coupling Catalyst. Chemistry-A European Journal, 12(18), 4749-4755.
  • [23] O'Brien, C. J., Kantchev, E. A. B., Valente, C., Hadei, N., Chass, G. A., Lough, A., Organ, M. G. 2006. Easily Prepared Air‐and Moisture‐Stable Pd–NHC (NHC= N‐Heterocyclic Carbene) Complexes: A Reliable, User‐Friendly, Highly Active Palladium Precatalyst for the Suzuki–Miyaura Reaction. Chemistry-a European Journal, 12(18), 4743-4748.
  • [24] Doǧan, Ö., Demir, S., Özdemir, İ., Cetinkaya, B. 2011. Palladium (II) NHC complexes containing benzimidazole ligand as a catalyst for C-N bond formation. Applied Organometallic Chemistry, 25(3), 163-167.
Toplam 24 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Mühendislik
Bölüm Makaleler
Yazarlar

Neslihan Şahin

Yayımlanma Tarihi 5 Ekim 2018
Yayımlandığı Sayı Yıl 2018 Cilt: 22 Sayı: Özel

Kaynak Göster

APA Şahin, N. (2018). Dikloro [1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil) benzimidazol-2-iliden] piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 22, 105-109.
AMA Şahin N. Dikloro [1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil) benzimidazol-2-iliden] piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi. SDÜ Fen Bil Enst Der. Ekim 2018;22:105-109.
Chicago Şahin, Neslihan. “Dikloro [1-(2-Metil-2-Propenil)-3-(3,4,5-Trimetoksibenzil) Benzimidazol-2-Iliden] Piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura Ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi”. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi 22, Ekim (Ekim 2018): 105-9.
EndNote Şahin N (01 Ekim 2018) Dikloro [1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil) benzimidazol-2-iliden] piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi 22 105–109.
IEEE N. Şahin, “Dikloro [1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil) benzimidazol-2-iliden] piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi”, SDÜ Fen Bil Enst Der, c. 22, ss. 105–109, 2018.
ISNAD Şahin, Neslihan. “Dikloro [1-(2-Metil-2-Propenil)-3-(3,4,5-Trimetoksibenzil) Benzimidazol-2-Iliden] Piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura Ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi”. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi 22 (Ekim 2018), 105-109.
JAMA Şahin N. Dikloro [1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil) benzimidazol-2-iliden] piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi. SDÜ Fen Bil Enst Der. 2018;22:105–109.
MLA Şahin, Neslihan. “Dikloro [1-(2-Metil-2-Propenil)-3-(3,4,5-Trimetoksibenzil) Benzimidazol-2-Iliden] Piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura Ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi”. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi, c. 22, 2018, ss. 105-9.
Vancouver Şahin N. Dikloro [1-(2-metil-2-propenil)-3-(3,4,5-trimetoksibenzil) benzimidazol-2-iliden] piridin paladyum(II) Kompleksinin Sentezi, Yapısal Karakterizasyonu, Suzuki-Miyaura ve Mizoroki-Heck Eşleşme Tepkimelerindeki Katalitik Aktivitesi. SDÜ Fen Bil Enst Der. 2018;22:105-9.

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