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101. Peng J-B, Wu F-P, Wu X-F (2019) First-row transition-metal-catalyzed carbonylative transformations of carbon electrophiles. Chem Rev 119(4):2090–2127. https://doi.org/10.1021/
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structure, electrochemistry, and application in catalytic coupling of terminal alkynes with
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104. Prabhu RN, Ramesh R (2016) Square-planar Ni(II) thiosemicarbazonato complex as an easily
accessible and convenient catalyst for Sonogashira cross-coupling reaction. Tetrahedron Lett
57(44):4893–4897. https://doi.org/10.1016/j.tetlet.2016.09.049
105. Prechtl MHG (ed) (2017) Nanocatalysis in ionic liquids. Wiley-VCH, Weinheim
106. Reina A, Favier I, Pradel C, Gómez M (2018) Stable Zero-Valent nickel nanoparticles in glycerol: synthesis and applications in selective hydrogenations. Adv Synth Catal
360(18):3544–3552. https://doi.org/10.1002/adsc.201800786
107. Roucoux A, Schulz J, Patin H (2002) Reduced transition metal colloids: a novel family of
reusable catalysts? Chem Rev 102(10):3757–3778. https://doi.org/10.1021/cr010350j
108. Safari J, Javadian L (2015) Ultrasound assisted green synthesis of 2-amino-4H-chromene
derivatives catalyzed by Fe 3 O 4 -functionalized nanoparticles with chitosan as a novel
and reusable magnetic catalyst. Ultrason Sonochem 22:341–348. https://doi.org/10.1016/j.
ultsonch.2014.02.002
109. Sambiagio C, Marsden SP, Blacker AJ, McGowan PC (2014) Copper catalysed Ullmann type
chemistry: from mechanistic aspects to modern development. Chem Soc Rev 43(10):3525–
3550. https://doi.org/10.1039/C3CS60289C
110. San K, Shon Y-S (2018) Synthesis of Alkanethiolate-capped Metal nanoparticles using alkyl
thiosulfate ligand precursors: a method to generate promising reagents for selective catalysis.
Nanomaterials 8(5):346. https://doi.org/10.3390/nano8050346
111. Schmid G (ed) (2011) Nanoparticles: from theory to application. Wiley-VCH, Weinheim
112. Serp P, Philippot K (eds) (2012) Nanomaterials in Catalysis. Wiley-VCH, Weinheim
113. Shaabani A, Afshari R (2018) Magnetic Ugi-functionalized graphene oxide complexed with
copper nanoparticles: Efficient catalyst toward Ullman coupling reaction in deep eutectic
solvents. J Colloid Interface Sci 510:384–394. https://doi.org/10.1016/j.jcis.2017.09.089
M. Camats et al.
95. Mondal P, Bhanja P, Khatun R, Bhaumik A, Das D, Manirul Islam S (2017) Palladium nanoparticles embedded on mesoporous TiO 2 material (Pd@MTiO 2 ) as an efficient heterogeneous catalyst for Suzuki-Coupling reactions in water medium. J Colloid Interface Sci 508:378–386.
https://doi.org/10.1016/j.jcis.2017.08.046
96. Nakamura E, Hatakeyama T, Ito S, Ishizuka K, Ilies L, Nakamura M (2013) Iron-catalyzed
cross-coupling reactions. Org React 1–210
97. Nasrollahzadeh M, Sajjadi M, Ghorbannezhad F, Sajadi SM (2018) A review on recent
advances in the application of nanocatalysts in A3 coupling reactions. Chem Rec 18(10):1409–
1473. https://doi.org/10.1002/tcr.201700100
98. Neiva EGC, Bergamini MF, Oliveira MM, Marcolino LH, Zarbin AJG (2014) PVP-capped
nickel nanoparticles: synthesis, characterization and utilization as a glycerol electrosensor.
Sens Actuator B Chem 196:574–581. https://doi.org/10.1016/j.snb.2014.02.041
99. Park J, Kang E, Son SU, Park HM, Lee MK, Kim J, Hyeon T (2005) Monodisperse nanoparticles of Ni and NiO: synthesis, characterization, self-assembled superlattices, and catalytic
applications in the Suzuki coupling reaction. Adv Mater 17(4):429–434. https://doi.org/10.
1002/adma.200400611
100. Patete JM, Peng X, Koenigsmann C, Xu Y, Karn B, Wong SS (2011) Viable methodologies
for the synthesis of high-quality nanostructures. Green Chem 13(3):482–519. https://doi.org/
10.1039/C0GC00516A
101. Peng J-B, Wu F-P, Wu X-F (2019) First-row transition-metal-catalyzed carbonylative transformations of carbon electrophiles. Chem Rev 119(4):2090–2127. https://doi.org/10.1021/
acs.chemrev.8b00068
102. Pozharskii AF, Soldatenkov AT, Katritzky AR (2011) Heterocycles in industry and technology.
In: Pozharskii AF, Soldatenkov AT, Katritzky AR (eds) Heterocycles in life and society, pp
209–246
103. Prabhu RN, Lakshmipraba J (2017) A nickel(II) thiosemicarbazonato complex: synthesis,
structure, electrochemistry, and application in catalytic coupling of terminal alkynes with
arylboronic acids. Transit Metal Chem 42(7):579–585. https://doi.org/10.1007/s11243-0170162-8
104. Prabhu RN, Ramesh R (2016) Square-planar Ni(II) thiosemicarbazonato complex as an easily
accessible and convenient catalyst for Sonogashira cross-coupling reaction. Tetrahedron Lett
57(44):4893–4897. https://doi.org/10.1016/j.tetlet.2016.09.049
105. Prechtl MHG (ed) (2017) Nanocatalysis in ionic liquids. Wiley-VCH, Weinheim
106. Reina A, Favier I, Pradel C, Gómez M (2018) Stable Zero-Valent nickel nanoparticles in glycerol: synthesis and applications in selective hydrogenations. Adv Synth Catal
360(18):3544–3552. https://doi.org/10.1002/adsc.201800786
107. Roucoux A, Schulz J, Patin H (2002) Reduced transition metal colloids: a novel family of
reusable catalysts? Chem Rev 102(10):3757–3778. https://doi.org/10.1021/cr010350j
108. Safari J, Javadian L (2015) Ultrasound assisted green synthesis of 2-amino-4H-chromene
derivatives catalyzed by Fe 3 O 4 -functionalized nanoparticles with chitosan as a novel
and reusable magnetic catalyst. Ultrason Sonochem 22:341–348. https://doi.org/10.1016/j.
ultsonch.2014.02.002
109. Sambiagio C, Marsden SP, Blacker AJ, McGowan PC (2014) Copper catalysed Ullmann type
chemistry: from mechanistic aspects to modern development. Chem Soc Rev 43(10):3525–
3550. https://doi.org/10.1039/C3CS60289C
110. San K, Shon Y-S (2018) Synthesis of Alkanethiolate-capped Metal nanoparticles using alkyl
thiosulfate ligand precursors: a method to generate promising reagents for selective catalysis.
Nanomaterials 8(5):346. https://doi.org/10.3390/nano8050346
111. Schmid G (ed) (2011) Nanoparticles: from theory to application. Wiley-VCH, Weinheim
112. Serp P, Philippot K (eds) (2012) Nanomaterials in Catalysis. Wiley-VCH, Weinheim
113. Shaabani A, Afshari R (2018) Magnetic Ugi-functionalized graphene oxide complexed with
copper nanoparticles: Efficient catalyst toward Ullman coupling reaction in deep eutectic
solvents. J Colloid Interface Sci 510:384–394. https://doi.org/10.1016/j.jcis.2017.09.089