8 Earth-Abundant d-Block Metal Nanocatalysis for Coupling …
275
41. Favier I, Pla D, Gómez M (2019) Palladium nanoparticles in polyols: synthesis, catalytic
couplings and hydrogenations. Chem Rev. https://doi.org/10.1021/acs.chemrev.9b00204
42. Favier I, Toro M-L, Lecante P, Pla D, Gómez M (2018) Palladium-mediated radical homocoupling reactions: a surface catalytic insight. Catal Sci Technol 8(18):4766–4773. https://
doi.org/10.1039/C8CY00901E
43. Fiévet F, Ammar-Merah S, Brayner R, Chau F, Giraud M, Mammeri F, Viau G (2018)
The polyol process: a unique method for easy access to metal nanoparticles with tailored
sizes, shapes and compositions. Chem Soc Rev 47(14):5187–5233. https://doi.org/10.1039/
C7CS00777A
44. Fievet F, Lagier JP, Blin B, Beaudoin B, Figlarz M (1989) Homogeneous and heterogeneous
nucleations in the polyol process for the preparation of micron and submicron size metal
particles. Solid State Ion 32–33:198–205. https://doi.org/10.1016/0167-2738(89)90222-1
45. Fievet F, Lagier JP, Figlarz M (2013) Preparing monodisperse metal powders in micrometer
and submicrometer sizes by the polyol process. MRS Bull 14(12):29–34. https://doi.org/10.
1557/S0883769400060930
46. Firouzabadi H, Iranpoor N, Gholinejad M, Hoseini J (2011) Magnetite (Fe 3 O 4 ) nanoparticlescatalyzed sonogashira-hagihara reactions in ethylene glycol under ligand-free conditions. Adv
Synth Catal 353(1):125–132. https://doi.org/10.1002/adsc.201000390
47. Firouzabadi H, Iranpoor N, Gholinejad M, Hoseini J (2011b) Magnetite (Fe 3 O 4 )
nanoparticles-catalyzed Sonogashira-Hagihara reactions in ethylene glycol under ligand-free
conditions. [Erratum to document cited in CA154:310261]. Adv Synth Catal 353(7):1027.
https://doi.org/10.1002/adsc.201190017
48. Formenti D, Ferretti F, Scharnagl FK, Beller M (2019) Reduction of nitro compounds
using 3d-non-noble metal catalysts. Chem Rev 119(4):2611–2680. https://doi.org/10.1021/
acs.chemrev.8b00547
49. Frindy S, El Kadib A, Lahcini M, Primo A, Garcia H (2015) Copper nanoparticles stabilized in
a porous chitosan aerogel as a heterogeneous catalyst for C-S cross-coupling. ChemCatChem
7(20):3307–3315. https://doi.org/10.1002/cctc.201500565
50. Gandeepan P, Müller T, Zell D, Cera G, Warratz S, Ackermann L (2019) 3d transition metals for
C-H activation. Chem Rev 119(4):2192–2452. https://doi.org/10.1021/acs.chemrev.8b00507
51. Ganem B (2009) Strategies for innovation in multicomponent reaction design. Acc Chem Res
42(3):463–472. https://doi.org/10.1021/ar800214s
52. Gawande MB, Goswami A, Felpin F-X, Asefa T, Huang X, Silva R, Varma RS (2016) Cu and
Cu-based nanoparticles: synthesis and applications in catalysis. Chem Rev 116(6):3722–3811.
https://doi.org/10.1021/acs.chemrev.5b00482
53. Ghiasbeigi E, Soleiman-Beigi M (2019) Copper immobilized on isonicotinic acid hydrazide
functionalized nano-magnetite as a novel recyclable catalyst for direct synthesis of phenols
and anilines. Chem Select 4(12):3611–3619. https://doi.org/10.1002/slct.201803770
54. Gholinejad M, Zareh F, Najera C (2018) Nitro group reduction and Suzuki reaction catalysed
by palladium supported on magnetic nanoparticles modified with carbon quantum dots generated from glycerol and urea. Appl Organomet Chem 32(1):e3984. https://doi.org/10.1002/
aoc.3984
55. Ghorbani-Choghamarani A, Tahmasbi B, Moradi P (2016) Palladium-S-propyl-2aminobenzothioate immobilized on Fe3O4 magnetic nanoparticles as catalyst for Suzuki
and Heck reactions in water or poly(ethylene glycol). Appl Organomet Chem 30(6):422–430.
https://doi.org/10.1002/aoc.3449
56. Ghosh Chaudhuri R, Paria S (2012) Core/shell nanoparticles: classes, properties, synthesis
mechanisms, characterization, and applications. Chem Rev 112(4):2373–2433. https://doi.
org/10.1021/cr100449n
57. Gilman H, Lichtenwalter M (1939) Relative reactivities of organometallic compounds. XXV.
Coupling reaction with halides of group VIII metals. J Am Chem Soc 61(4):957–959. https://
doi.org/10.1021/ja01873a056
58. Grasso S, Micale N, Monforte A-M, Monforte P, Polimeni S, Zappalà M (2000) Synthesis
and in vitro antitumour activity evaluation of 1-aryl-1H,3H-thiazolo[4,3-b]quinazolines. Eur
J Med Chem 35(12):1115–1119. https://doi.org/10.1016/S0223-5234(00)01195-8
275
41. Favier I, Pla D, Gómez M (2019) Palladium nanoparticles in polyols: synthesis, catalytic
couplings and hydrogenations. Chem Rev. https://doi.org/10.1021/acs.chemrev.9b00204
42. Favier I, Toro M-L, Lecante P, Pla D, Gómez M (2018) Palladium-mediated radical homocoupling reactions: a surface catalytic insight. Catal Sci Technol 8(18):4766–4773. https://
doi.org/10.1039/C8CY00901E
43. Fiévet F, Ammar-Merah S, Brayner R, Chau F, Giraud M, Mammeri F, Viau G (2018)
The polyol process: a unique method for easy access to metal nanoparticles with tailored
sizes, shapes and compositions. Chem Soc Rev 47(14):5187–5233. https://doi.org/10.1039/
C7CS00777A
44. Fievet F, Lagier JP, Blin B, Beaudoin B, Figlarz M (1989) Homogeneous and heterogeneous
nucleations in the polyol process for the preparation of micron and submicron size metal
particles. Solid State Ion 32–33:198–205. https://doi.org/10.1016/0167-2738(89)90222-1
45. Fievet F, Lagier JP, Figlarz M (2013) Preparing monodisperse metal powders in micrometer
and submicrometer sizes by the polyol process. MRS Bull 14(12):29–34. https://doi.org/10.
1557/S0883769400060930
46. Firouzabadi H, Iranpoor N, Gholinejad M, Hoseini J (2011) Magnetite (Fe 3 O 4 ) nanoparticlescatalyzed sonogashira-hagihara reactions in ethylene glycol under ligand-free conditions. Adv
Synth Catal 353(1):125–132. https://doi.org/10.1002/adsc.201000390
47. Firouzabadi H, Iranpoor N, Gholinejad M, Hoseini J (2011b) Magnetite (Fe 3 O 4 )
nanoparticles-catalyzed Sonogashira-Hagihara reactions in ethylene glycol under ligand-free
conditions. [Erratum to document cited in CA154:310261]. Adv Synth Catal 353(7):1027.
https://doi.org/10.1002/adsc.201190017
48. Formenti D, Ferretti F, Scharnagl FK, Beller M (2019) Reduction of nitro compounds
using 3d-non-noble metal catalysts. Chem Rev 119(4):2611–2680. https://doi.org/10.1021/
acs.chemrev.8b00547
49. Frindy S, El Kadib A, Lahcini M, Primo A, Garcia H (2015) Copper nanoparticles stabilized in
a porous chitosan aerogel as a heterogeneous catalyst for C-S cross-coupling. ChemCatChem
7(20):3307–3315. https://doi.org/10.1002/cctc.201500565
50. Gandeepan P, Müller T, Zell D, Cera G, Warratz S, Ackermann L (2019) 3d transition metals for
C-H activation. Chem Rev 119(4):2192–2452. https://doi.org/10.1021/acs.chemrev.8b00507
51. Ganem B (2009) Strategies for innovation in multicomponent reaction design. Acc Chem Res
42(3):463–472. https://doi.org/10.1021/ar800214s
52. Gawande MB, Goswami A, Felpin F-X, Asefa T, Huang X, Silva R, Varma RS (2016) Cu and
Cu-based nanoparticles: synthesis and applications in catalysis. Chem Rev 116(6):3722–3811.
https://doi.org/10.1021/acs.chemrev.5b00482
53. Ghiasbeigi E, Soleiman-Beigi M (2019) Copper immobilized on isonicotinic acid hydrazide
functionalized nano-magnetite as a novel recyclable catalyst for direct synthesis of phenols
and anilines. Chem Select 4(12):3611–3619. https://doi.org/10.1002/slct.201803770
54. Gholinejad M, Zareh F, Najera C (2018) Nitro group reduction and Suzuki reaction catalysed
by palladium supported on magnetic nanoparticles modified with carbon quantum dots generated from glycerol and urea. Appl Organomet Chem 32(1):e3984. https://doi.org/10.1002/
aoc.3984
55. Ghorbani-Choghamarani A, Tahmasbi B, Moradi P (2016) Palladium-S-propyl-2aminobenzothioate immobilized on Fe3O4 magnetic nanoparticles as catalyst for Suzuki
and Heck reactions in water or poly(ethylene glycol). Appl Organomet Chem 30(6):422–430.
https://doi.org/10.1002/aoc.3449
56. Ghosh Chaudhuri R, Paria S (2012) Core/shell nanoparticles: classes, properties, synthesis
mechanisms, characterization, and applications. Chem Rev 112(4):2373–2433. https://doi.
org/10.1021/cr100449n
57. Gilman H, Lichtenwalter M (1939) Relative reactivities of organometallic compounds. XXV.
Coupling reaction with halides of group VIII metals. J Am Chem Soc 61(4):957–959. https://
doi.org/10.1021/ja01873a056
58. Grasso S, Micale N, Monforte A-M, Monforte P, Polimeni S, Zappalà M (2000) Synthesis
and in vitro antitumour activity evaluation of 1-aryl-1H,3H-thiazolo[4,3-b]quinazolines. Eur
J Med Chem 35(12):1115–1119. https://doi.org/10.1016/S0223-5234(00)01195-8