21. Noyori R (2002) Asymmetric catalysis: science and opportunities (Nobel lecture). Angew
Chem Int Ed 41:2008–2022
22. Lawrence MAW, Green K-A, Nelson PN, Lorraine SC (2018) Review: pincer ligands –
tunable, versatile and applicable. Polyhedron 143:11–27
23. Hetterscheid DGH, van der Vlugt JI, de Bruin B, Reek JNH (2009) Water splitting by
cooperative catalysis. Angew Chem Int Ed 48:8178–8181
24. Bouhadir G, Bourissou D (2017) Coordination of Lewis acids to transition metals: Z-type
ligands. In: Mingos DMP (ed) The chemical bond III: 100 years old and getting stronger.
Springer, Cham, pp 141–201
25. Amgoune A, Bourissou D (2011) σ-acceptor, Z-type ligands for transition metals. Chem
Commun 47:859–871
26. You D, Gabbaï FP (2019) Tunable σ-accepting, Z-type ligands for organometallic catalysis.
Trends Chem 1:485–496
27. Owen GR (2016) Functional group migrations between boron and metal centres within
transition metal–borane and –boryl complexes and cleavage of H–H, E–H and E–E
0 bonds.
Chem Commun 52:10712–10726
28. Braunschweig H, Dewhurst RD (2011) Transition metals as Lewis bases: “Z-type” boron
ligands and metal-to-boron dative bonding. Dalton Trans 40:549–558
29. Kameo H, Nakazawa H (2013) Recent developments in the coordination chemistry of
multidentate ligands featuring a boron moiety. Chem Asian J 8:1720–1734
30. Verhoeven DGA, Moret M-E (2016) Metal–ligand cooperation at tethered π-ligands. Dalton
Trans 45:15762–15778
31. Bouhadir G, Bourissou D (2016) Complexes of ambiphilic ligands: reactivity and catalytic
applications. Chem Soc Rev 45:1065–1079
32. van Koten G, Timmer K, Noltes JG, Spek AL (1978) A novel type of Pt–C interaction and a
model for the final stage in reductive elimination processes involving C–C coupling at Pt;
synthesis and molecular geometry of [1,N,N
0 -η-2,6-bis{(dimethylamino)methyl}-toluene]
iodoplatinum(II) tetrafluoroborate. J Chem Soc Chem Commun:250–252
33. Choi J, MacArthur AHR, Brookhart M, Goldman AS (2011) Dehydrogenation and related
reactions catalyzed by iridium pincer complexes. Chem Rev 111:1761–1779
34. Albrecht M, van Koten G (2001) Platinum group organometallics based on “pincer” complexes: sensors, switches, and catalysts. Angew Chem Int Ed 40:3750–3781
35. Kirchner K (2015) Pincer and pincer-type complexes applications in organic synthesis and
catalysis. Edited by Kálmán J. Szabó and Ola F. Wendt. Angew Chem Int Ed 54:4706–4707
36. Allen KE, Heinekey DM, Goldman AS, Goldberg KI (2013) Alkane dehydrogenation by C–H
activation at iridium(III). Organometallics 32:1579–1582
37. Tanaka R, Yamashita M, Nozaki K (2009) Catalytic hydrogenation of carbon dioxide using Ir
(III)Àpincer complexes. J Am Chem Soc 131:14168–14169
38. Martín M, Sola E (2020) Chapter two – recent advances in the chemistry of group 9 – pincer
organometallics. In: Pérez PJ (ed) Advances in organometallic chemistry. Academic Press, pp
79–193
39. Morales-Morales D (2018) Pincer compounds chemistry and applications. Elsevier,
Amsterdam
40. Li H, Gonçalves TP, Lupp D, Huang K-W (2019) PN3(P)-pincer complexes: cooperative
catalysis and beyond. ACS Catal 9:1619–1629
41. van Koten G, Milstein D (2013) Organometallic pincer chemistry. Springer, Berlin
42. Asay M, Morales-Morales D (2015) Non-symmetric pincer ligands: complexes and applications in catalysis. Dalton Trans 44:17432–17447
43. Lyaskovskyy V, de Bruin B (2012) Redox non-innocent ligands: versatile new tools to control
catalytic reactions. ACS Catal 2:270–279
44. Gunanathan C, Milstein D (2011) Metal–ligand cooperation by aromatization–
dearomatization: a new paradigm in bond activation and “Green” catalysis. Acc Chem Res
44:588–602
Metal-Ligand Cooperation at Phosphine-Based Acceptor Pincer Ligands
65
Chem Int Ed 41:2008–2022
22. Lawrence MAW, Green K-A, Nelson PN, Lorraine SC (2018) Review: pincer ligands –
tunable, versatile and applicable. Polyhedron 143:11–27
23. Hetterscheid DGH, van der Vlugt JI, de Bruin B, Reek JNH (2009) Water splitting by
cooperative catalysis. Angew Chem Int Ed 48:8178–8181
24. Bouhadir G, Bourissou D (2017) Coordination of Lewis acids to transition metals: Z-type
ligands. In: Mingos DMP (ed) The chemical bond III: 100 years old and getting stronger.
Springer, Cham, pp 141–201
25. Amgoune A, Bourissou D (2011) σ-acceptor, Z-type ligands for transition metals. Chem
Commun 47:859–871
26. You D, Gabbaï FP (2019) Tunable σ-accepting, Z-type ligands for organometallic catalysis.
Trends Chem 1:485–496
27. Owen GR (2016) Functional group migrations between boron and metal centres within
transition metal–borane and –boryl complexes and cleavage of H–H, E–H and E–E
0 bonds.
Chem Commun 52:10712–10726
28. Braunschweig H, Dewhurst RD (2011) Transition metals as Lewis bases: “Z-type” boron
ligands and metal-to-boron dative bonding. Dalton Trans 40:549–558
29. Kameo H, Nakazawa H (2013) Recent developments in the coordination chemistry of
multidentate ligands featuring a boron moiety. Chem Asian J 8:1720–1734
30. Verhoeven DGA, Moret M-E (2016) Metal–ligand cooperation at tethered π-ligands. Dalton
Trans 45:15762–15778
31. Bouhadir G, Bourissou D (2016) Complexes of ambiphilic ligands: reactivity and catalytic
applications. Chem Soc Rev 45:1065–1079
32. van Koten G, Timmer K, Noltes JG, Spek AL (1978) A novel type of Pt–C interaction and a
model for the final stage in reductive elimination processes involving C–C coupling at Pt;
synthesis and molecular geometry of [1,N,N
0 -η-2,6-bis{(dimethylamino)methyl}-toluene]
iodoplatinum(II) tetrafluoroborate. J Chem Soc Chem Commun:250–252
33. Choi J, MacArthur AHR, Brookhart M, Goldman AS (2011) Dehydrogenation and related
reactions catalyzed by iridium pincer complexes. Chem Rev 111:1761–1779
34. Albrecht M, van Koten G (2001) Platinum group organometallics based on “pincer” complexes: sensors, switches, and catalysts. Angew Chem Int Ed 40:3750–3781
35. Kirchner K (2015) Pincer and pincer-type complexes applications in organic synthesis and
catalysis. Edited by Kálmán J. Szabó and Ola F. Wendt. Angew Chem Int Ed 54:4706–4707
36. Allen KE, Heinekey DM, Goldman AS, Goldberg KI (2013) Alkane dehydrogenation by C–H
activation at iridium(III). Organometallics 32:1579–1582
37. Tanaka R, Yamashita M, Nozaki K (2009) Catalytic hydrogenation of carbon dioxide using Ir
(III)Àpincer complexes. J Am Chem Soc 131:14168–14169
38. Martín M, Sola E (2020) Chapter two – recent advances in the chemistry of group 9 – pincer
organometallics. In: Pérez PJ (ed) Advances in organometallic chemistry. Academic Press, pp
79–193
39. Morales-Morales D (2018) Pincer compounds chemistry and applications. Elsevier,
Amsterdam
40. Li H, Gonçalves TP, Lupp D, Huang K-W (2019) PN3(P)-pincer complexes: cooperative
catalysis and beyond. ACS Catal 9:1619–1629
41. van Koten G, Milstein D (2013) Organometallic pincer chemistry. Springer, Berlin
42. Asay M, Morales-Morales D (2015) Non-symmetric pincer ligands: complexes and applications in catalysis. Dalton Trans 44:17432–17447
43. Lyaskovskyy V, de Bruin B (2012) Redox non-innocent ligands: versatile new tools to control
catalytic reactions. ACS Catal 2:270–279
44. Gunanathan C, Milstein D (2011) Metal–ligand cooperation by aromatization–
dearomatization: a new paradigm in bond activation and “Green” catalysis. Acc Chem Res
44:588–602
Metal-Ligand Cooperation at Phosphine-Based Acceptor Pincer Ligands
65