8 Earth-Abundant d-Block Metal Nanocatalysis for Coupling …
273
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1. Adil SF, Assal ME, Khan M, Al-Warthan A, Siddiqui MRH, Liz-Marzán LM (2015) Biogenic synthesis of metallic nanoparticles and prospects toward green chemistry. Dalton Trans
44(21):9709–9717. https://doi.org/10.1039/C4DT03222E
2. Ai W, Zhong R, Liu X, Liu Q (2019) Hydride Transfer reactions catalyzed by cobalt complexes.
Chem Rev 119(4):2876–2953. https://doi.org/10.1021/acs.chemrev.8b00404
3. Alice W, Axel Jacobi von W (2013) Iron(0) nanoparticle catalysts in organic synthesis. Curr
Org Chem 17(4):326–335. https://doi.org/10.2174/1385272811317040003
4. Alig L, Fritz M, Schneider S (2019) First-row transition metal (de)hydrogenation catalysis
based on functional pincer ligands. Chem Rev 119(4):2681–2751. https://doi.org/10.1021/
acs.chemrev.8b00555
5. An K, Alayoglu S, Ewers T, Somorjai GA (2012) Colloid chemistry of nanocatalysts:
a molecular view. J Colloid Interface Sci 373(1):1–13. https://doi.org/10.1016/j.jcis.2011.
10.082
6. Anastas P, Eghbali N (2010) Green chemistry: principles and practice. Chem Soc Rev
39(1):301–312. https://doi.org/10.1039/B918763B
7. Anastas PT, Warner JC (2000) Green chemistry. Oxford University Press, New York
8. Anastas PT, Zimmerman JB (2003) Peer reviewed: design through the 12 principles of green
engineering. Environ Sci Technol 37(5):94A–101A. https://doi.org/10.1021/es032373g
9. Anastas PT, Kirchhoff MM, Williamson TC (2001) Catalysis as a foundational pillar of green
chemistry. Appl Catal A 221(1):3–13. https://doi.org/10.1016/S0926-860X(01)00793-1
10. Astruc D (ed) (2008) Nanoparticles and catalysis. Wiley
11. Bedford RB (2015) How low does iron go? Chasing the active species in fe-catalyzed crosscoupling reactions. Acc Chem Res 48(5):1485–1493. https://doi.org/10.1021/acs.accounts.
5b00042
12. Bedford RB, Betham M, Bruce DW, Davis SA, Frost RM, Hird M (2006) Iron nanoparticles
in the coupling of alkyl halides with aryl Grignard reagents. Chem Commun 13:1398–1400.
https://doi.org/10.1039/b601014h
13. Bedford RB, Brenner PB (2015) The development of iron catalysts for cross-coupling
reactions. In: Bauer E (ed) Iron catalysis II. Springer International Publishing, Cham, pp
19–46
14. Beletskaya IP, Cheprakov AV (2004) Copper in cross-coupling reactions: the post-Ullmann
chemistry. Coord Chem Rev 248(21):2337–2364. https://doi.org/10.1016/j.ccr.2004.09.014
15. Beletskaya IP, Latyshev GV, Tsvetkov AV, Lukashev NV (2003) The nickel-catalyzed
Sonogashira-Hagihara reaction. Tetrahedron Lett 44(27):5011–5013. https://doi.org/10.1016/
S0040-4039(03)01174-2
16. Beller M (2019) Introduction: first row metals and catalysis. Chem Rev 119(4):2089. https://
doi.org/10.1021/acs.chemrev.9b00076
17. Bhosale MA, Sasaki T, Bhanage BM (2014) A facile and rapid route for the synthesis of
Cu/Cu 2 O nanoparticles and their application in the Sonogashira coupling reaction of acyl
chlorides with terminal alkynes. Catal Sci Technol 4(12):4274–4280. https://doi.org/10.1039/
C4CY00868E
18. Biffis A, Centomo P, Del Zotto A, Zecca 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.7b00443
19. Biggs-Houck JE, Younai A, Shaw JT (2010) Recent advances in multicomponent reactions for
diversity-oriented synthesis. Curr Opin Chem Biol 14(3):371–382. https://doi.org/10.1016/j.
cbpa.2010.03.003
20. Boettger R (1859) Ueber die Einwirkung des Leuchtgases auf verschiedene Salzsolutionen, insbesondere auf eine ammoniakalische Kupferchlorürlösung. Justus Liebigs Ann Chem
109(3):351–362. https://doi.org/10.1002/jlac.18591090318
273
References
1. Adil SF, Assal ME, Khan M, Al-Warthan A, Siddiqui MRH, Liz-Marzán LM (2015) Biogenic synthesis of metallic nanoparticles and prospects toward green chemistry. Dalton Trans
44(21):9709–9717. https://doi.org/10.1039/C4DT03222E
2. Ai W, Zhong R, Liu X, Liu Q (2019) Hydride Transfer reactions catalyzed by cobalt complexes.
Chem Rev 119(4):2876–2953. https://doi.org/10.1021/acs.chemrev.8b00404
3. Alice W, Axel Jacobi von W (2013) Iron(0) nanoparticle catalysts in organic synthesis. Curr
Org Chem 17(4):326–335. https://doi.org/10.2174/1385272811317040003
4. Alig L, Fritz M, Schneider S (2019) First-row transition metal (de)hydrogenation catalysis
based on functional pincer ligands. Chem Rev 119(4):2681–2751. https://doi.org/10.1021/
acs.chemrev.8b00555
5. An K, Alayoglu S, Ewers T, Somorjai GA (2012) Colloid chemistry of nanocatalysts:
a molecular view. J Colloid Interface Sci 373(1):1–13. https://doi.org/10.1016/j.jcis.2011.
10.082
6. Anastas P, Eghbali N (2010) Green chemistry: principles and practice. Chem Soc Rev
39(1):301–312. https://doi.org/10.1039/B918763B
7. Anastas PT, Warner JC (2000) Green chemistry. Oxford University Press, New York
8. Anastas PT, Zimmerman JB (2003) Peer reviewed: design through the 12 principles of green
engineering. Environ Sci Technol 37(5):94A–101A. https://doi.org/10.1021/es032373g
9. Anastas PT, Kirchhoff MM, Williamson TC (2001) Catalysis as a foundational pillar of green
chemistry. Appl Catal A 221(1):3–13. https://doi.org/10.1016/S0926-860X(01)00793-1
10. Astruc D (ed) (2008) Nanoparticles and catalysis. Wiley
11. Bedford RB (2015) How low does iron go? Chasing the active species in fe-catalyzed crosscoupling reactions. Acc Chem Res 48(5):1485–1493. https://doi.org/10.1021/acs.accounts.
5b00042
12. Bedford RB, Betham M, Bruce DW, Davis SA, Frost RM, Hird M (2006) Iron nanoparticles
in the coupling of alkyl halides with aryl Grignard reagents. Chem Commun 13:1398–1400.
https://doi.org/10.1039/b601014h
13. Bedford RB, Brenner PB (2015) The development of iron catalysts for cross-coupling
reactions. In: Bauer E (ed) Iron catalysis II. Springer International Publishing, Cham, pp
19–46
14. Beletskaya IP, Cheprakov AV (2004) Copper in cross-coupling reactions: the post-Ullmann
chemistry. Coord Chem Rev 248(21):2337–2364. https://doi.org/10.1016/j.ccr.2004.09.014
15. Beletskaya IP, Latyshev GV, Tsvetkov AV, Lukashev NV (2003) The nickel-catalyzed
Sonogashira-Hagihara reaction. Tetrahedron Lett 44(27):5011–5013. https://doi.org/10.1016/
S0040-4039(03)01174-2
16. Beller M (2019) Introduction: first row metals and catalysis. Chem Rev 119(4):2089. https://
doi.org/10.1021/acs.chemrev.9b00076
17. Bhosale MA, Sasaki T, Bhanage BM (2014) A facile and rapid route for the synthesis of
Cu/Cu 2 O nanoparticles and their application in the Sonogashira coupling reaction of acyl
chlorides with terminal alkynes. Catal Sci Technol 4(12):4274–4280. https://doi.org/10.1039/
C4CY00868E
18. Biffis A, Centomo P, Del Zotto A, Zecca 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.7b00443
19. Biggs-Houck JE, Younai A, Shaw JT (2010) Recent advances in multicomponent reactions for
diversity-oriented synthesis. Curr Opin Chem Biol 14(3):371–382. https://doi.org/10.1016/j.
cbpa.2010.03.003
20. Boettger R (1859) Ueber die Einwirkung des Leuchtgases auf verschiedene Salzsolutionen, insbesondere auf eine ammoniakalische Kupferchlorürlösung. Justus Liebigs Ann Chem
109(3):351–362. https://doi.org/10.1002/jlac.18591090318