A novel polymer containing phosphorus–nitrogen ligands for stabilization of palladium nanoparticles: an efficient and recyclable catalyst for Suzuki and Sonogashira reactions in neat water

Highly monodispersed palladium nanoparticles supported on polymer containing phosphorus and nitrogen ligands was successfully synthesized, characterized and used in Suzuki and Sonogashira coupling reactions in water.

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Correction: A novel polymer containing phosphorus–nitrogen ligands for stabilization of palladium nanoparticles: an efficient and recyclable catalyst for Suzuki and Sonogashira reactions in neat water

Dalton Transactions ◽

10.1039/c9dt90055a ◽

2019 ◽

Vol 48 (12) ◽

pp. 4067-4069

Author(s):

M. Gholinejad ◽

F. Hamed ◽

P. Biji

Keyword(s):

Palladium Nanoparticles ◽

Recyclable Catalyst ◽

Dalton Trans ◽

Nitrogen Ligands ◽

Neat Water ◽

Sonogashira Reactions

Correction for ‘A novel polymer containing phosphorus–nitrogen ligands for stabilization of palladium nanoparticles: an efficient and recyclable catalyst for Suzuki and Sonogashira reactions in neat water’ by M. Gholinejad, et al., Dalton Trans., 2015, 44, 14293–14303.

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Palladium nanoparticles decorated on a novel polyazomethine as a highly productive and recyclable catalyst for Suzuki coupling reactions and 4-nitrophenol reduction

Journal of Organometallic Chemistry ◽

10.1016/j.jorganchem.2019.120886 ◽

2019 ◽

Vol 899 ◽

pp. 120886 ◽

Cited By ~ 3

Author(s):

Nuray Yılmaz Baran

Keyword(s):

Palladium Nanoparticles ◽

Suzuki Coupling ◽

Recyclable Catalyst ◽

Coupling Reactions ◽

Nitrophenol Reduction

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Sonogashira coupling reactions: Synthesis of 4-substituted-6-methyl-2-(methylthio)pyrimidines catalyzed by Pd–Cu

Journal of Chemical Research ◽

10.1177/1747519819868920 ◽

2019 ◽

Vol 43 (9-10) ◽

pp. 431-436

Author(s):

Fatemeh Rezaeimanesh ◽

Mohammad Bakherad ◽

Hossein Nasr-Isfahani

Keyword(s):

Efficient Method ◽

Room Temperature ◽

Reaction Times ◽

Coupling Reactions ◽

Sonogashira Coupling ◽

Aryl Iodides ◽

Palladium Catalyzed ◽

Sonogashira Reactions

An efficient method is developed for the synthesis of 4-(3-arylprop-2-ynyloxy)-6-methyl-2-(methylthio)pyrimidines via palladium-catalyzed Sonogashira reactions of 4-methyl-2-(methylthio)-6-(prop-2-yn-1-yloxy)pyrimidine with electron-poor aryl iodides in acetonitrile at room temperature. Excellent yields of the products were obtained in reaction times of 9–11 h.

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Pd complex of an NNN pincer ligand supported on γ-Fe2O3@SiO2 magnetic nanoparticles: a new catalyst for Heck, Suzuki and Sonogashira coupling reactions

New Journal of Chemistry ◽

10.1039/c5nj00344j ◽

2015 ◽

Vol 39 (9) ◽

pp. 7076-7085 ◽

Cited By ~ 49

Author(s):

Sara Sobhani ◽

Zohre Zeraatkar ◽

Farzaneh Zarifi

Keyword(s):

Magnetic Nanoparticles ◽

Recyclable Catalyst ◽

Coupling Reactions ◽

Sonogashira Coupling ◽

Pincer Ligand ◽

Magnetically Recyclable Catalyst

Pd-BIP-γ-Fe2O3@SiO2 was used successfully as an air- and moisture-stable magnetically recyclable catalyst for Heck, Suzuki and Sonogashira coupling reactions.

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Biosynthesis of palladium nanoparticles using Rosa canina fruit extract and their use as a heterogeneous and recyclable catalyst for Suzuki-Miyaura coupling reactions in water

Applied Organometallic Chemistry ◽

10.1002/aoc.3421 ◽

2016 ◽

Vol 30 (4) ◽

pp. 231-235 ◽

Cited By ~ 74

Author(s):

Hojat Veisi ◽

Asra Rashtiani ◽

Venous Barjasteh

Keyword(s):

Palladium Nanoparticles ◽

Recyclable Catalyst ◽

Coupling Reactions ◽

Fruit Extract ◽

Rosa Canina

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Palladium nanoparticles supported on agarose-functionalized magnetic nanoparticles of Fe3O4 as a recyclable catalyst for C–C bond formation via Suzuki–Miyaura, Heck–Mizoroki and Sonogashira–Hagihara coupling reactions

RSC Advances ◽

10.1039/c4ra00900b ◽

2014 ◽

Vol 4 (33) ◽

pp. 17060-17070 ◽

Cited By ~ 58

Author(s):

Habib Firouzabadi ◽

Nasser Iranpoor ◽

Mohammad Gholinejad ◽

Samira Akbari ◽

Neda Jeddi

Keyword(s):

Magnetic Nanoparticles ◽

Palladium Nanoparticles ◽

Bond Formation ◽

Recyclable Catalyst ◽

Coupling Reactions ◽

Functionalized Magnetic Nanoparticles ◽

Bond Formation Reactions

Palladium nanoparticles supported on agarose functionalized Fe3O4 catalyzed C–C bond formation reactions.

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Palladium nanoparticles supported on poly (N-vinylpyrrolidone)-grafted silica as new recyclable catalyst for Heck cross-coupling reactions

Journal of Organometallic Chemistry ◽

10.1016/j.jorganchem.2010.09.028 ◽

2011 ◽

Vol 696 (2) ◽

pp. 594-599 ◽

Cited By ~ 55

Author(s):

Bahman Tamami ◽

Hamed Allahyari ◽

Soheila Ghasemi ◽

Fatemeh Farjadian

Keyword(s):

Palladium Nanoparticles ◽

Cross Coupling ◽

Recyclable Catalyst ◽

Coupling Reactions ◽

Cross Coupling Reactions

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Xylan-type hemicellulose supported palladium nanoparticles: a highly efficient and reusable catalyst for the carbon–carbon coupling reactions

Catalysis Science & Technology ◽

10.1039/c3cy00933e ◽

2014 ◽

Vol 4 (5) ◽

pp. 1426-1435 ◽

Cited By ~ 24

Author(s):

Wei Chen ◽

Lin-xin Zhong ◽

Xin-wen Peng ◽

Kun Wang ◽

Zhi-feng Chen ◽

...

Keyword(s):

Heterogeneous Catalyst ◽

Palladium Nanoparticles ◽

Cross Coupling ◽

Recyclable Catalyst ◽

Reusable Catalyst ◽

Coupling Reactions ◽

Highly Efficient ◽

Cross Coupling Reactions ◽

Supported Palladium

A heterogeneous catalyst was prepared by depositing palladium nanoparticles onto xylan-type hemicellulose, which is a kind of renewable biopolymer catalyst, and used as an efficient and recyclable catalyst for the Suzuki, Heck, and Sonogashira cross-coupling reactions.

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