Synthesis and photoluminescence studies of siloles with arylene ethynylene strands
C Ding, G Babu, A Orita, T Hirate, J Otera
Index: Ding, Changhua; Babu, Govindarajulu; Orita, Akihiro; Hirate, Takayoshi; Otera, Junzo Synlett, 2007 , # 16 p. 2559 - 2563
Full Text: HTML
Citation Number: 13
Abstract
Abstract Siloles attached to phenylene ethynylene strands were prepared successfully by Sonogashira coupling of 2, 5-dibromosilole with ethyne-terminated phenylene ethynylenes. Elongation of the arylene ethynylene chain involving up to at least three aromatic rings leads to high quantum yields in solution.
Related Articles:
[Lyapkalo, Ilya M.; Vogel, Michael A. K.; Boltukhina, Ekaterina V.; Vavrik, Jiri Synlett, 2009 , # 4 p. 558 - 561]
Novel 3-phenylprop-2-ynylamines as inhibitors of mammalian squalene epoxidase
[Organic and biomolecular chemistry, , vol. 1, # 3 p. 498 - 506]
[Bioorganic and Medicinal Chemistry Letters, , vol. 18, # 3 p. 954 - 958]
Derivatives of 2-arylcyclopropylamine: Synthesis and interactions with 5-HT 1A receptors.
[Bioorganic and Medicinal Chemistry Letters, , vol. 6, # 4 p. 415 - 420]
A convenient synthesis of 1-bromoolefins and acetylenes by a chain extension of aldehydes
[Tetrahedron Letters, , vol. 21, p. 4021 - 4024]