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Original Articles

Synthesis and redox properties of sterically crowded triarylphosphine bearing two phenothiazine moieties

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Pages 598-601 | Received 01 Oct 2018, Accepted 06 Nov 2018, Published online: 20 Feb 2019

References

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  • (a) Sasaki, S.; Murakami, F.; Murakami, M.; Watanabe, M.; Kato, K.; Sutoh, K.; Yoshifuji, M. Synthesis of Crowded Triarylphosphines Carrying Functional Sites. J. Organomet. Chem. 2005, 690, 2664–2672. (b) Sutoh, K.; Sasaki, S.; Yoshifuji, M. Synthesis and Redox Properties of Crowded Triarylphosphines Possessing Ferrocenyl Groups. Inorg. Chem. 2006, 45, 992–998. (c) Sasaki, S.; Sasaki, K.; Yoshifuji, M. Synthesis, Structure, and Properties of Tris(2,6-diisopropyl-4-methoxyphenyl)phosphine. Phosphorus Sulfur Silicon Relat. Elem. 2008, 183, 410–414. (d) Sasaki, S.; Murakami, M.; Murakami, F.; Yoshifuji, M. Synthesis and Redox Properties of Sterically Crowded Triarylphosphine and Tetraaryldiphosphane Bearing Phenothiazinyl Groups. Heteroatom Chem. 2011, 22, 506–513.
  • (a) Sasaki, S.; Ogawa, K.; Watanabe, M.; Yoshifuji, M. Synthesis and Properties of Sterically Crowded Triarylphosphines Bearing Naphthoquinone Moieties. Organometallics 2010, 29, 757–766. (b) Sasaki, S.; Sasaki, K.; Yoshifuji, M. Synthesis, Structure, and Properties of Extended πp-Conjugated Systems Bearing Sterically Crowded Triarylphosphines. J. Organomet. Chem. 2011, 696, 3307–3315. (c) Sasaki, S.; Ogawa, K.; Nakamura, K.; Yoshifuji, M.; Morita, N. Synthesis and Properties of Sterically Crowded Triarylphosphines Bearing Anthra- and Naphtho- quinones, and Their Oligomers. J. Organomet. Chem. 2014, 751, 525–533. (d) Sasaki, S. Sterically Crowded Triarylphosphines Bearing Cyano Groups. Tetrahedron Lett. 2018, 59, 2250–2254.
  • Sasaki, S.; Kato, K.; Yoshifuji, M. Synthesis and Redox Properties of Crowded Triarylphosphines Carrying a Nitroxide Radical and Related Compounds. Bull. Chem. Soc. Jpn. 2007, 80, 1791–1798.

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