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Erschienen in: Topics in Catalysis 14/2018

20.08.2018 | Original Paper

Pd(II)–Ni(II) Pyrazolate Framework as Active and Recyclable Catalyst for the Hydroamination of Terminal Alkynes

verfasst von: Francisco G. Cirujano, Elena López-Maya, J. A. R. Navarro, Dirk E. De Vos

Erschienen in: Topics in Catalysis | Ausgabe 14/2018

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Abstract

Well-dispersed [Pd(NH3)4]2+ sites have been introduced in the defective nickel pyrazolate porous framework, known as K@NiBDP. The resulting porous crystalline material shows a superior catalytic behavior for C–N bond formations than [Pd(NH3)4]2+ containing zeolite HY. The palladium exchanged catalyst, Pd@NiBDP, is able to promote both intra- and intermolecular hydroamination of terminal alkynes with excellent activity, reusability and selectivity towards the corresponding indole or imine versus the hydration of the alkyne. The same Pd species introduced in the microporous acid HY zeolite favors the hydration of the terminal alkyne towards the corresponding ketone, instead of the addition of the amine to the triple bond.

Graphical Abstract

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Literatur
1.
Zurück zum Zitat Taylor AP, Robinson RP, Fobian YM, Blakemore DC, Jones LH, Fadeyi O (2016) Modern advances in heterocyclic chemistry in drug discovery. Org Biomol Chem 14:6611–6637CrossRefPubMed Taylor AP, Robinson RP, Fobian YM, Blakemore DC, Jones LH, Fadeyi O (2016) Modern advances in heterocyclic chemistry in drug discovery. Org Biomol Chem 14:6611–6637CrossRefPubMed
2.
Zurück zum Zitat Bechtoldt A, Tirler C, Raghuvanshi K, Warratz S, Kornhaaß C, Ackermann L (2016) Ruthenium oxidase catalysis for site-selective C–H alkenylations with ambient O2 as the sole oxidant. Angew Chem Int Ed 55:264–267CrossRef Bechtoldt A, Tirler C, Raghuvanshi K, Warratz S, Kornhaaß C, Ackermann L (2016) Ruthenium oxidase catalysis for site-selective C–H alkenylations with ambient O2 as the sole oxidant. Angew Chem Int Ed 55:264–267CrossRef
3.
Zurück zum Zitat Ackermann L (2005) General and efficient indole syntheses based on catalytic amination reactions. Org Lett 7:439–442CrossRefPubMed Ackermann L (2005) General and efficient indole syntheses based on catalytic amination reactions. Org Lett 7:439–442CrossRefPubMed
4.
Zurück zum Zitat Ackermann L, Barfüßer S, Potukuchi HK (2009) Copper-catalyzed N-arylation/hydroamination domino synthesis of indoles and its application to the preparation of a chek1/KDR kinase inhibitor pharmacophore. Adv Synth Catal 351:1064–1072CrossRef Ackermann L, Barfüßer S, Potukuchi HK (2009) Copper-catalyzed N-arylation/hydroamination domino synthesis of indoles and its application to the preparation of a chek1/KDR kinase inhibitor pharmacophore. Adv Synth Catal 351:1064–1072CrossRef
5.
Zurück zum Zitat Ackermann L, Althammer A (2007) Domino N-H/C-H bond activation: palladium-catalyzed synthesis of annulated heterocycles using dichloro(hetero)arenes. Angew Chem Int Ed 46:1627–1629CrossRef Ackermann L, Althammer A (2007) Domino N-H/C-H bond activation: palladium-catalyzed synthesis of annulated heterocycles using dichloro(hetero)arenes. Angew Chem Int Ed 46:1627–1629CrossRef
6.
Zurück zum Zitat Gates BC (2016) Concluding remarks: progress toward the design of solid catalysts. Faraday Discuss 188:591–602CrossRefPubMed Gates BC (2016) Concluding remarks: progress toward the design of solid catalysts. Faraday Discuss 188:591–602CrossRefPubMed
7.
Zurück zum Zitat Cirujano FG (2017) MOFs vs. zeolites: carbonyl activation with M(IV) catalytic sites. Catal Sci Technol 7:5482–5494CrossRef Cirujano FG (2017) MOFs vs. zeolites: carbonyl activation with M(IV) catalytic sites. Catal Sci Technol 7:5482–5494CrossRef
8.
Zurück zum Zitat Santoro S, Kozhushkov SI, Ackermann L, Vaccaro L (2016) Heterogeneous catalytic approaches in C–H activation reactions. Green Chem 18:3471–3493CrossRef Santoro S, Kozhushkov SI, Ackermann L, Vaccaro L (2016) Heterogeneous catalytic approaches in C–H activation reactions. Green Chem 18:3471–3493CrossRef
9.
Zurück zum Zitat Alonso F, Beletskaya IP, Yus M (2005) Non-conventional methodologies for transition-metal catalysed carbon-carbon coupling: a critical overview. Tetrahedron 61:11771–11835CrossRef Alonso F, Beletskaya IP, Yus M (2005) Non-conventional methodologies for transition-metal catalysed carbon-carbon coupling: a critical overview. Tetrahedron 61:11771–11835CrossRef
10.
Zurück zum Zitat Sachtler WMH, Cavalcanti FAP (1991) Coordination, atom reorganization, and catalysis of palladium in zeolite cages. Catal Lett 9:261–271CrossRef Sachtler WMH, Cavalcanti FAP (1991) Coordination, atom reorganization, and catalysis of palladium in zeolite cages. Catal Lett 9:261–271CrossRef
11.
Zurück zum Zitat Sachtler WMH (1993) Metal clusters in zeolites: an intriguing class of catalysts. Acc Chem Res 26:383–387CrossRef Sachtler WMH (1993) Metal clusters in zeolites: an intriguing class of catalysts. Acc Chem Res 26:383–387CrossRef
12.
Zurück zum Zitat Djakovitch L, Rollet P (2004) Adv Synth Catal 346(13–15):1782–1792CrossRef Djakovitch L, Rollet P (2004) Adv Synth Catal 346(13–15):1782–1792CrossRef
13.
Zurück zum Zitat Djakovitch L, Dufaud V, Zaidi R (2006) Heterogeneous palladium catalysts applied to the synthesis of 2- and 2,3-functionalised indoles. Adv Synth Catal 348(6):715–724CrossRef Djakovitch L, Dufaud V, Zaidi R (2006) Heterogeneous palladium catalysts applied to the synthesis of 2- and 2,3-functionalised indoles. Adv Synth Catal 348(6):715–724CrossRef
14.
Zurück zum Zitat Djakovitch L, Rouge P (2007) New homogeneously and heterogeneously [Pd/Cu]-catalysed C3-alkenylation of free NH-indoles. J Mol Catal A 273:230–239CrossRef Djakovitch L, Rouge P (2007) New homogeneously and heterogeneously [Pd/Cu]-catalysed C3-alkenylation of free NH-indoles. J Mol Catal A 273:230–239CrossRef
15.
Zurück zum Zitat Li H, Zhu Z, Zhang F, Xie S, Li H, Li P, Zhou X (2011) Palladium nanoparticles confined in the cages of MIL-101: an efficient catalyst for the one-pot indole synthesis in water. ACS Catal 1:1604–1612CrossRef Li H, Zhu Z, Zhang F, Xie S, Li H, Li P, Zhou X (2011) Palladium nanoparticles confined in the cages of MIL-101: an efficient catalyst for the one-pot indole synthesis in water. ACS Catal 1:1604–1612CrossRef
16.
Zurück zum Zitat Manna K, Zhang T, Lin W (2014) Postsynthetic metalation of bipyridyl-containing metal–organic frameworks for highly efficient catalytic organic transformations. J Am Chem Soc 136:6566–6569CrossRefPubMed Manna K, Zhang T, Lin W (2014) Postsynthetic metalation of bipyridyl-containing metal–organic frameworks for highly efficient catalytic organic transformations. J Am Chem Soc 136:6566–6569CrossRefPubMed
17.
Zurück zum Zitat Huang YB, Shen M, Wang X, Huang P, Chen R, Lin ZJ, Cao R (2016) Water-medium C–H activation over a hydrophobic perfluoroalkane-decorated metal-organic framework platform. J Catal 333:1–7CrossRef Huang YB, Shen M, Wang X, Huang P, Chen R, Lin ZJ, Cao R (2016) Water-medium C–H activation over a hydrophobic perfluoroalkane-decorated metal-organic framework platform. J Catal 333:1–7CrossRef
18.
Zurück zum Zitat López-Maya E, Montoro C, Colombo V, Barea E, Navarro JAR (2014) Improved CO2 capture from flue gas by basic sites, charge gradients, and missing linker defects on nickel face cubic centered MOFs. Adv Funct Mater 24:6130–6135CrossRef López-Maya E, Montoro C, Colombo V, Barea E, Navarro JAR (2014) Improved CO2 capture from flue gas by basic sites, charge gradients, and missing linker defects on nickel face cubic centered MOFs. Adv Funct Mater 24:6130–6135CrossRef
19.
Zurück zum Zitat Montoro C, Ocõn P, Zamora F, Navarro JAR (2016) Metal–organic frameworks containing missing-linker defects leading to high hydroxide-ion conductivity chem. Eur J 22:1646–1651CrossRef Montoro C, Ocõn P, Zamora F, Navarro JAR (2016) Metal–organic frameworks containing missing-linker defects leading to high hydroxide-ion conductivity chem. Eur J 22:1646–1651CrossRef
20.
Zurück zum Zitat Rodríguez-Albelo LM, López-Maya E, Hamad S, Ruiz-Salvador R, Calero S, Navarro JAR (2017) Selective sulfur dioxide adsorption on crystal defect sites on an isoreticular metal organic framework series. Nat Commun 8:14457CrossRefPubMedPubMedCentral Rodríguez-Albelo LM, López-Maya E, Hamad S, Ruiz-Salvador R, Calero S, Navarro JAR (2017) Selective sulfur dioxide adsorption on crystal defect sites on an isoreticular metal organic framework series. Nat Commun 8:14457CrossRefPubMedPubMedCentral
21.
Zurück zum Zitat Cirujano FG, López-Maya E, Rodríguez-Albelo M, Barea E, Navarro JAR, De Vos DE (2017) Selective one-pot two-step C–C bond formation using metal–organic frameworks with mild basicity as heterogeneous catalysts. ChemCatChem 9:4019–4023CrossRef Cirujano FG, López-Maya E, Rodríguez-Albelo M, Barea E, Navarro JAR, De Vos DE (2017) Selective one-pot two-step C–C bond formation using metal–organic frameworks with mild basicity as heterogeneous catalysts. ChemCatChem 9:4019–4023CrossRef
22.
Zurück zum Zitat Djakovitch L, Koehler K (2001) Heck reaction catalyzed by Pd-modified zeolites. J Am Chem Soc 123:5990–5999CrossRefPubMed Djakovitch L, Koehler K (2001) Heck reaction catalyzed by Pd-modified zeolites. J Am Chem Soc 123:5990–5999CrossRefPubMed
23.
Zurück zum Zitat Noel S, Luo C, Pinel C, Djakovitch L (2007) efficient heterogeneously palladium-catalysed Heck arylation of acrolein diethyl acetal. Selective synthesis of cinnamaldehydes or 3-arylpropionic esters. Adv Synth Catal 349(7):1128–1140CrossRef Noel S, Luo C, Pinel C, Djakovitch L (2007) efficient heterogeneously palladium-catalysed Heck arylation of acrolein diethyl acetal. Selective synthesis of cinnamaldehydes or 3-arylpropionic esters. Adv Synth Catal 349(7):1128–1140CrossRef
24.
Zurück zum Zitat Augustyniak AW, Zawartka W, Navarro JAR, Trzeciak AM (2016) Palladium nanoparticles supported on a nickel pyrazolate metal organic framework as a catalyst for Suzuki and carbonylative Suzuki couplings. Dalton Trans 45:13525–13531CrossRefPubMed Augustyniak AW, Zawartka W, Navarro JAR, Trzeciak AM (2016) Palladium nanoparticles supported on a nickel pyrazolate metal organic framework as a catalyst for Suzuki and carbonylative Suzuki couplings. Dalton Trans 45:13525–13531CrossRefPubMed
25.
Zurück zum Zitat Fortea-Pérez FR, Mon M, Ferrando-Soria J, Boronat M, Leyva-Pérez A, Corma A, Herrera JM, Osadchii D, Gascon J, Armentano D, Pardo E (2017) The MOF-driven synthesis of supported palladium clusters with catalytic activity for carbene-mediated chemistry. Nat Mater 16:760–766PubMed Fortea-Pérez FR, Mon M, Ferrando-Soria J, Boronat M, Leyva-Pérez A, Corma A, Herrera JM, Osadchii D, Gascon J, Armentano D, Pardo E (2017) The MOF-driven synthesis of supported palladium clusters with catalytic activity for carbene-mediated chemistry. Nat Mater 16:760–766PubMed
26.
Zurück zum Zitat Mueller TE, Hultzsch KC, Yus M, Foubelo F, Tada M (2008) Hydroamination: direct addition of amines to alkenes and alkynes. Chem Rev 108:3795–3892CrossRef Mueller TE, Hultzsch KC, Yus M, Foubelo F, Tada M (2008) Hydroamination: direct addition of amines to alkenes and alkynes. Chem Rev 108:3795–3892CrossRef
27.
Zurück zum Zitat Penzien J, Haeßner C, Jentys A, Köhler K, Müller TE, Lercher JA (2004) Heterogeneous catalysts for hydroamination reactions: structure–activity relationship. J Catal 221:302–312CrossRef Penzien J, Haeßner C, Jentys A, Köhler K, Müller TE, Lercher JA (2004) Heterogeneous catalysts for hydroamination reactions: structure–activity relationship. J Catal 221:302–312CrossRef
28.
Zurück zum Zitat Rubio-Marqués P, Rivero-Crespo MA, Leyva-Pérez A, Corma A (2015) Well-defined noble metal single sites in zeolites as an alternative to catalysis by insoluble metal salts. J Am Chem Soc 137:11832–11837CrossRefPubMed Rubio-Marqués P, Rivero-Crespo MA, Leyva-Pérez A, Corma A (2015) Well-defined noble metal single sites in zeolites as an alternative to catalysis by insoluble metal salts. J Am Chem Soc 137:11832–11837CrossRefPubMed
29.
Zurück zum Zitat Marquez C, Rivera-Torrente M, Paalanen PP, Weckhuysen BM, Cirujano FG, De Vos D, De Baerdemaeker T (2017) Increasing the availability of active sites in Zn-Co double metal cyanides by dispersion onto a SiO2 support. J Catal 354:92–99CrossRef Marquez C, Rivera-Torrente M, Paalanen PP, Weckhuysen BM, Cirujano FG, De Vos D, De Baerdemaeker T (2017) Increasing the availability of active sites in Zn-Co double metal cyanides by dispersion onto a SiO2 support. J Catal 354:92–99CrossRef
30.
Zurück zum Zitat Perry CH, Athans DP, Young EF (1967) Far infrared spectra of palladium compounds. Spectrochim Acta 173:1137–1147CrossRef Perry CH, Athans DP, Young EF (1967) Far infrared spectra of palladium compounds. Spectrochim Acta 173:1137–1147CrossRef
31.
Zurück zum Zitat Cabrero-Antonino JR, Leyva-Pérez A, Corma A (2015) Beyond acid strength in zeolites: soft framework counteranions for stabilization of carbocations on zeolites and its implication in organic synthesis. Angew Chem Int Ed 54:5658–5661CrossRef Cabrero-Antonino JR, Leyva-Pérez A, Corma A (2015) Beyond acid strength in zeolites: soft framework counteranions for stabilization of carbocations on zeolites and its implication in organic synthesis. Angew Chem Int Ed 54:5658–5661CrossRef
33.
Zurück zum Zitat Liu W, Wang H, Li CJ (2016) Metal-free markovnikov-type alkyne hydration under mild conditions. Org Lett 18:2184–2187CrossRefPubMed Liu W, Wang H, Li CJ (2016) Metal-free markovnikov-type alkyne hydration under mild conditions. Org Lett 18:2184–2187CrossRefPubMed
34.
Zurück zum Zitat La Sorella G, Sperni L, Ballester P, Strukula G, Scarso A (2016) Hydration of aromatic alkynes catalyzed by a self-assembled hexameric organic capsule. Catal Sci Technol 6:6031–6036CrossRef La Sorella G, Sperni L, Ballester P, Strukula G, Scarso A (2016) Hydration of aromatic alkynes catalyzed by a self-assembled hexameric organic capsule. Catal Sci Technol 6:6031–6036CrossRef
35.
Zurück zum Zitat Sing KSW, Everett DH, Haul RAW, Moscou L, Pierotti RA, Rouquerol J, Siemieniewska T (1985) Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity. Pure Appl Chem 57:603–619CrossRef Sing KSW, Everett DH, Haul RAW, Moscou L, Pierotti RA, Rouquerol J, Siemieniewska T (1985) Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity. Pure Appl Chem 57:603–619CrossRef
36.
Zurück zum Zitat Chen Q, Lv L, Yu M, Shi Y, Li Y, Pang G. Cao C (2013) Simple, efficient and reusable Pd–NHC catalysts for hydroamination. RSC Adv 3:18359–18366CrossRef Chen Q, Lv L, Yu M, Shi Y, Li Y, Pang G. Cao C (2013) Simple, efficient and reusable Pd–NHC catalysts for hydroamination. RSC Adv 3:18359–18366CrossRef
Metadaten
Titel
Pd(II)–Ni(II) Pyrazolate Framework as Active and Recyclable Catalyst for the Hydroamination of Terminal Alkynes
verfasst von
Francisco G. Cirujano
Elena López-Maya
J. A. R. Navarro
Dirk E. De Vos
Publikationsdatum
20.08.2018
Verlag
Springer US
Erschienen in
Topics in Catalysis / Ausgabe 14/2018
Print ISSN: 1022-5528
Elektronische ISSN: 1572-9028
DOI
https://doi.org/10.1007/s11244-018-1039-6

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