Synthesis of palladium supported on mesoporous hydroxyapatite from oyster shells for use as efficient, green, and recyclable catalyst for Heck reactions
Source abstract
Abstract
Homogeneous catalysts exhibit several drawbacks, such as high cost, difficulty of separation, and non-recyclability, necessitating the development of heterogenous catalysts to solve these problems. Hydroxyapatite (HAP) can be used as a catalyst carrier owing to its surface acid–base adjustability and strong ion exchange properties. Oyster shell is one of the primary natural sources of hydroxyapatite. The use of cuttlefish bone as a source of hydroxyapatite can also facilitate the recycling of bone waste and reduce the consumption of scarce biological resources and limit environmental pollution. In this study, a heterogeneous catalyst was synthesized by the immobilization of Pd on hydroxyapatite obtained by the hydrothermal method using naturally abundant oyster shells as the calcium source, ammonium dibasic phosphate as the phosphorus source, and cetyltrimethylammonium bromide as the porogen. The synthesized heterogeneous catalyst was characterized using N2-physisorption (adsorption–desorption) measurements, X-ray diffraction analysis, X-ray photoelectron spectroscopy, inductively coupled plasma mass spectrometry, transmission electron microscopy, and temperature-programmed reduction and desorption measurements. The Pd/HAP catalyst shows high catalytic activity for the cross-coupling reaction between iodobenzene and olefins, resulting in yields greater than 67%. Moreover, the Pd/HAP catalyst could be recycled and reused six times with slight reduction in the yield, and thus, is highly stable and recyclable. In addition, it is suitable for use in Heck cross-coupling reactions between various aryl halides and alkenes. Thus, the synthesized catalyst should find extensive use in synthetic chemistry. Graphical abstract
Source: expertdata · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nanomaterials for catalytic reactions · Catalytic Cross-Coupling Reactions · Asymmetric Hydrogenation and Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (55)
Show source-provided references
1. Arpad M (2011) Efficient, selective, and recyclable palladium catalysts in carbon-carbon coupling reactions. Chem Rev 111(3):2251–2320. https://doi.org/10.1021/cr100355b10.1021/cr100355b ↗
2. Barakat NAM, Khil MS, Omran AM, Sheikh FA, Kim HY (2009) Extraction of pure natural hydroxyapatite from the bovine bones bio waste by three different methods. J Mater Process Technol 209(7):3408–3415. https://doi.org/10.1016/j.jmatprotec.2008.07.04010.1016/j.jmatprotec.2008.07.040 ↗
3. Bianchi CL, Canton P, Dimitratos N, Porta F, Prati L (2005) Selective oxidation of glycerol with oxygen using mono and bimetallic catalysts based on Au, Pd and Pt metals. Catal Today 102:203–212. https://doi.org/10.1016/j.cattod.2005.02.00310.1016/j.cattod.2005.02.003 ↗
4. Biffis A, Centomo P, Del Zotto A, Zeccal M (2018) Pd metal catalysts for cross-couplings and related reactions in the 21st century: a critical review. Chem Rev 118(4):2249–2295. https://doi.org/10.1021/acs.chemrev.7b0044310.1021/acs.chemrev.7b00443 ↗
5. Bose S, Saha SK (2003) Synthesis and characterization of hydroxyapatite nanopowders by emulsion technique. Chem Mater 15(23):4464–4469. https://doi.org/10.1021/cm030343710.1021/cm0303437 ↗
6. Boukha Z, Gil-Calvo M, de Rivas B, Gonzalez-Velasco JR, Gutierrez-Ortiz JI, Lopez-Fonseca R (2018) Behaviour of Rh supported on hydroxyapatite catalysts in partial oxidation and steam reforming of methane: on the role of the speciation of the Rh particles. Appl Catal A-Gen 556:191–203. https://doi.org/10.1016/j.apcata.2018.03.00210.1016/j.apcata.2018.03.002 ↗
7. Chai YC, Shang WX, Li WJ, Wu GJ, Dai WL, Guan NJ, Li LD (2019) Nobel metal particles confined in zeolites: synthesis, characterization, and applications. Adv Sci 6(16):19. https://doi.org/10.1002/advs.20190029910.1002/advs.201900299 ↗
8. Chambyal OS, Paul S, Shamim T, Gupta M, Gupta R, Loupy A (2013) HAP-Pd(0): a highly efficient recyclable heterogeneous catalyst for the selective reduction of carbon-carbon double bond in alpha, beta-unsaturated ketones. Synth Commun 43(5):656–667. https://doi.org/10.1080/00397911.2011.60524210.1080/00397911.2011.605242 ↗
9. Chen ZP, Vorobyeva E, Mitchell S, Fako E, Ortuno MA, Lopez N, Collins SM, Midgley PA, Richard S, Vile G, Perez-Ramirez J (2018) A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling. Nat Nanotechnol. 13(8):702. https://doi.org/10.1038/s41565-018-0167-210.1038/s41565-018-0167-2 ↗
10. Chinchilla R, Najera C (2014) Chemicals from alkynes with palladium catalysts. Chem Rev 114(3):1783–1826. https://doi.org/10.1021/cr400133p10.1021/cr400133p ↗
11. Christoffel F, Ward TR (2018) Palladium-catalyzed heck cross-coupling reactions in water: a comprehensive review. Catal Lett 148(2):489–511. https://doi.org/10.1007/s10562-017-2285-010.1007/s10562-017-2285-0 ↗
12. Gayen A, Priolkar KR, Sarode R, Jayaram V, Hegde MS, Subbanna GN, Emura S (2004) Ce1-xRhxO2-delta solid solution formation in combustion-synthesized Rh/CeO2 catalyst studied by XRD, TEM, XPS, and EXAFS. Chem Mater 16(11):2317–2328. https://doi.org/10.1021/cm040126l10.1021/cm040126l ↗
13. Glasnov TN, Findenig S, Kappe CO (2009) Heterogeneous versus homogeneous palladium catalysts for ligandless Mizoroki-Heck reactions: a comparison of batch/microwave and continuous-flow processing. Chem Eur J 15(4):1001–1010. https://doi.org/10.1002/chem.20080220010.1002/chem.200802200 ↗
14. Indra A, Gopinath CS, Bhaduri S, Lahiri GK (2013) Hydroxyapatite supported palladium catalysts for Suzuki-Miyaura cross-coupling reaction in aqueous medium. Catal Sci Technol 3(6):1625–1633. https://doi.org/10.1039/c3cy00160a10.1039/c3cy00160a ↗
15. Johnson MFL, Mooi J (1987) Cerium dioxide crystallite sizes by temperature-programmed reduction. J Catal 103(2):502–505. https://doi.org/10.1016/0021-9517(87)90142-410.1016/0021-9517(87)90142-4 ↗
16. Kann N (2010) Recent applications of polymer supported organometallic catalysts in organic synthesis. Molecules 15(9):6306–6331. https://doi.org/10.3390/molecules1509630610.3390/molecules15096306 ↗
17. Karimi B, Behzadnia H, Farhangi E, Jafari E, Zamani A (2010) Recent application of polymer supported metal nanoparticles in Heck, Suzuki and Sonogashira coupling reactions. Curr Org Synth 7(6):543–567. https://doi.org/10.2174/15701791079432853810.2174/157017910794328538 ↗
18. Karnalanathan P, Ramesh S, Bang LT, Niakan A, Tan CY, Purbolaksono J, Chandran H, Teng WD (2014) Synthesis and sintering of hydroxyapatite derived from eggshells as a calcium precursor. Ceram Int 40(10):16349–16359. https://doi.org/10.1016/j.ceramint.2014.07.07410.1016/j.ceramint.2014.07.074 ↗
19. Khodaei MM, Dehghan M (2019) Palladium nanoparticles immobilized on Schiff base-functionalized mesoporous silica as a highly efficient and magnetically recoverable nanocatalyst for Heck coupling reaction. Appl Organomet Chem 33(1):9. https://doi.org/10.1002/aoc.461810.1002/aoc.4618 ↗
20. Kulagina MA, Gerasimov EY, Kardash TY, Simonov PA, Romanenko AV (2015) A universal method to form Pd nanoparticles on low-surface-area inorganic powders and their support-dependent catalytic activity in hydrogenation of maleic acid. Catal Today 246:72–80. https://doi.org/10.1016/j.cattod.2014.07.04810.1016/j.cattod.2014.07.048 ↗
21. Kumbhar A, Salunkhe R (2015) Recent advances in biopolymer supported palladium in organic synthesis. Curr Org Chem 19(21):2075–2121. https://doi.org/10.2174/138527281966615050518584310.2174/1385272819666150505185843 ↗
22. Li C, Xu G, Liu X, Zhang Y, Fu Y (2017) Hydrogenation of biomass-derived furfural to tetrahydrofurfuryl alcohol over hydroxyapatite-supported Pd catalyst under mild conditions. Ind Eng Chem Res 56(31):8843–8849. https://doi.org/10.1021/acs.iecr.7b0204610.1021/acs.iecr.7b02046 ↗
23. Liu LC, Corma A (2018) Metal catalysts for heterogeneous catalysis: from single atoms to nanoclusters and nanoparticles. Chem Rev 118(10):4981–5079. https://doi.org/10.1021/acs.chemrev.7b0077610.1021/acs.chemrev.7b00776 ↗
24. Lukic MJ, Sezen M, Veljovic D, Mrakovic A (2017) A facile route for hydroxyapatite densification with an increased heating rate. Mater Lett 207:12–15. https://doi.org/10.1016/j.matlet.2017.07.02010.1016/j.matlet.2017.07.020 ↗
25. Marques FL, Oliveira AC, Mendes Filho J, Rodriguez-Castellon E, Cavalcante CL Jr, Vieira RS (2015) Synthesis of lactic acid from glycerol using a Pd/C catalyst. Fuel Process Technol 138:228–235. https://doi.org/10.1016/j.fuproc.2015.05.03210.1016/j.fuproc.2015.05.032 ↗
26. Moghaddam FM, Pourkaveh R, Karimi A, Ayati SE (2018) Palladium immobilized onto functionalized magnetic nanoparticles as robust catalysts for amination and room-temperature Ullmann homocoupling of aryl halides: a walk around the C-F bond activation. Asian J Org Chem 7(4):802–809. https://doi.org/10.1002/ajoc.20180004110.1002/ajoc.201800041 ↗
27. Mora M, Jimenez-Sanchidrian C, Ruiz JR (2012) Recent advances in the heterogeneous palladium-catalysed Suzuki cross-coupling reaction. Curr Org Chem 16(9):1128–1150. https://doi.org/10.2174/13852721280056435810.2174/138527212800564358 ↗
28. Mori K, Hara T, Mizugaki T, Ebitani K, Kaneda K (2004) Hydroxyapatite-supported palladium nanoclusters: a highly active heterogeneous catalyst for selective oxidation of alcohols by use of molecular oxygen. J Am Chem Soc 126(34):10657–10666. https://doi.org/10.1021/ja048868310.1021/ja0488683 ↗
29. Nasrallah H, Hierso JC (2019) Porous materials based on 3-dimensional Td-directing functionalized adamantane scaffolds and applied as recyclable catalysts. Chem Mat 31(3):619–642. https://doi.org/10.1021/acs.chemmater.8b0450810.1021/acs.chemmater.8b04508 ↗
30. Nasrollahzadeh M, Atarod M, Alizadeh M, Hatamifard A, Sajadi SM (2017) Recent advances in the application of heterogeneous nanocaalysts for Sonogashira coupling reactions. Curr Org Chem 21(8):708–749. https://doi.org/10.2174/138527282066616102110294310.2174/1385272820666161021102943 ↗
31. Nasrollahzadeh M, Motahharifar N, Ghorbannezhad F, Bidgoli NSS, Baran T, Varma RS (2020) Recent advances in polymer supported palladium complexes as (nano) catalysts for Sonogashira coupling reaction. Mol Catal 480:31. https://doi.org/10.1016/j.mcat.2019.11064510.1016/j.mcat.2019.110645 ↗
32. Nayar S, Guha A (2009) Waste utilization for the controlled synthesis of nanosized hydroxyapatite. Mater Sci Eng C Biomim Supramol Syst 29(4):1326–1329. https://doi.org/10.1016/j.msec.2008.10.00210.1016/j.msec.2008.10.002 ↗
33. Padmanabhan SK, Balakrishnan A, Chu M-C, Lee YJ, Kim TN, Cho S-J (2009) Sol-gel synthesis and characterization of hydroxyapatite nanorods. Particuology 7(6):466–470. https://doi.org/10.1016/j.partic.2009.06.00810.1016/j.partic.2009.06.008 ↗
34. Perrichon V, Laachir A, Bergeret G, Fréty R, Tournayan L, Touret O (1994) Reduction of cerias with different textures by hydrogen and their reoxidation by oxygen. J Chem Soc Faraday Trans 90(5):773–781. https://doi.org/10.1039/FT994900077310.1039/FT9949000773 ↗
35. Pon-On W, Suntornsaratoon P, Charoenphandhu N, Thongbunchoo J, Krishnamra N, Tang IM (2016) Hydroxyapatite from fish scale for potential use as bone scaffold or regenerative material. Mater Sci Eng C Mater Biol Appl 62:183–189. https://doi.org/10.1016/j.msec.2016.01.05110.1016/j.msec.2016.01.051 ↗
36. Rafiee F (2019) Recent advances in the application of chitosan and chitosan derivatives as bio supported catalyst in the cross coupling reactions. Curr Org Chem 23(4):390–408. https://doi.org/10.2174/138527282366619031816422310.2174/1385272823666190318164223 ↗
37. Ray J, Anoop A, Ray D, Nasima Y, Sajal M, Ray P, Urinda S (2013) Palladium-catalyzed intramolecular oxidative Heck cyclization and its application toward a synthesis of (±)-β-cuparenone derivatives supported by computational studies. Synthesis 45(09):1261–1269. https://doi.org/10.1055/s-0032-131688410.1055/s-0032-1316884 ↗
38. Ray JK, Paul S, Ray P, Singha R, Rao DY, Nandi S, Anoop A (2017) Pd-catalyzed intramolecular sequential Heck cyclization and oxidation reactions: a facile pathway for the synthesis of substituted cycloheptenone evaluated using computational studies. New J Chem 41(1):278–284. https://doi.org/10.1039/c6nj02694j10.1039/c6nj02694j ↗
39. Ray JK, Singha R, Ray D, Ray P, Rao DY, Anoop A (2019) Palladium-catalyzed expedient Heck annulations in 1-bromo-1,5-dien-3-ols: Exceptional formation of fused bicycles. Tetrahedron Lett 60(13):931–935. https://doi.org/10.1016/j.tetlet.2019.02.04310.1016/j.tetlet.2019.02.043 ↗
40. Sangeetha P, Shanthi K, Rao KSR, Viswanathan B, Selvam P (2009) Hydrogenation of nitrobenzene over palladium-supported catalysts-effect of support. Appl Catal A Gen 353(2):160–165. https://doi.org/10.1016/j.apcata.2008.10.04410.1016/j.apcata.2008.10.044 ↗
41. Schmidt AF, Kurokhtina AA, Smirnov VV, Larina EV, Chechil EV (2012) competing reaction method for identification of fast and slow steps of catalytic cycles: application to heck and Suzuki reactions. Kinet Catal 53(2):214–221. https://doi.org/10.1134/s002315841202010310.1134/s0023158412020103 ↗
42. Seechurn C, Kitching MO, Colacot TJ, Snieckus V (2012) Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize. Angew Chem Int Edit 51(21):5062–5085. https://doi.org/10.1002/anie.20110701710.1002/anie.201107017 ↗
43. Shen Y, Zhang S, Li H, Ren Y, Liu H (2010) Efficient synthesis of lactic acid by aerobic oxidation of glycerol on Au-Pt/TiO2 catalysts. Chem A Eur J 16(25):7368–7371. https://doi.org/10.1002/chem.20100074010.1002/chem.201000740 ↗
44. Singha R, Roy S, Nandi S, Ray P, Ray JK (2013) Palladium-catalyzed one-pot Suzuki-Miyaura cross coupling followed by oxidative lactonization: a novel and efficient route for the one-pot synthesis of benzo c chromene-6-ones. Tetrahedron Lett 54(7):657–660. https://doi.org/10.1016/j.tetlet.2012.11.14410.1016/j.tetlet.2012.11.144 ↗
45. Tang H, Su Y, Guo Y, Zhang L, Li T, Zang K, Liu F, Li L, Luo J, Qiao B, Wang J (2018) Oxidative strong metal-support interactions (OMSI) of supported platinum-group metal catalysts. Chem Sci 9(32):6679–6684. https://doi.org/10.1039/c8sc01392f10.1039/c8sc01392f ↗
46. Tian PF, Ouyang L, Xu XY, Ao C, Xu XC, Si R, Shen XJ, Lin M, Xu J, Han YF (2017) The origin of palladium particle size effects in the direct synthesis of H2O2: is smaller better? J Catal 349:30–40. https://doi.org/10.1016/j.jcat.2016.12.00410.1016/j.jcat.2016.12.004 ↗
47. Venkatesan J, Rekha PD, Anil S, Bhatnagar I, Sudha PN, Dechsakulwatana C, Kim S-K, Shim MS (2018) Hydroxyapatite from cuttlefish bone: isolation, characterizations, and applications. Biotechnol Bioprocess Eng 23(4):383–393. https://doi.org/10.1007/s12257-018-0169-910.1007/s12257-018-0169-9 ↗
48. Wang Y, Zhao J, Wang X, Li Z, Liu P (2013) The complete oxidation of ethanol at low temperature over a novel Pd-Ce/gamma-Al2O3-TiO2 catalyst. Bull Korean Chem Soc 34(8):2461–2465. https://doi.org/10.5012/bkcs.2013.34.8.246110.5012/bkcs.2013.34.8.2461 ↗
49. Wang J, Huang SP, Hu K, Zhou KC, Sun H (2015) Effect of cetyltrimethylammonium bromide on morphology and porous structure of mesoporous hydroxyapatite. Trans Nonferrous Met Soc China 25(2):483–489. https://doi.org/10.1016/s1003-6326(15)63628-710.1016/s1003-6326(15)63628-7 ↗
50. Wang N, Sun QM, Yu JH (2019) Ultrasmall metal nanoparticles confined within crystalline nanoporous materials: a fascinating class of nanocatalysts. Adv Mater 31(1):23. https://doi.org/10.1002/adma.20180396610.1002/adma.201803966 ↗
51. Wu S-C, Hsu H-C, Hsu S-K, Tseng C-P, Ho W-F (2017) Preparation and characterization of hydroxyapatite synthesized from oyster shell powders. Adv Powder Technol 28(4):1154–1158. https://doi.org/10.1016/j.apt.2017.02.00110.1016/j.apt.2017.02.001 ↗
52. Yao HC, Yao YFY (1984) Ceria in automotive exhaust catalysts: I. Oxygen storage. J Catal 86(2):254–265. https://doi.org/10.1016/0021-9517(84)90371-310.1016/0021-9517(84)90371-3 ↗
53. Zeng F, Wang J, Wu Y, Yu Y, Tang W, Yin M, Liu C (2014) Preparation of pore expanded mesoporous hydroxyapatite via auxiliary solubilizing template method. Colloids Surf A Physicochem Eng Asp 441:737–743. https://doi.org/10.1016/j.colsurfa.2013.10.02810.1016/j.colsurfa.2013.10.028 ↗
54. Zhang C, Li C, Huang S, Hou Z, Cheng Z, Yang P, Peng C, Lin J (2010) Self-activated luminescent and mesoporous strontium hydroxyapatite nanorods for drug delivery. Biomaterials 31(12):3374–3383. https://doi.org/10.1016/j.biomaterials.2010.01.04410.1016/j.biomaterials.2010.01.044 ↗
55. Zhang Y, Zhu J, Li S, Xiao Y, Zhan Y, Wang X, Au C-T, Jiang L (2020) Rational design of highly H2O- and CO2-tolerant hydroxyapatite-supported Pd catalyst for low-temperature methane combustion. Chem Eng J 396:125225. https://doi.org/10.1016/j.cej.2020.12522510.1016/j.cej.2020.125225 ↗