1289037-84-8

Upstream product

• 1289037-82-6 C₄₄H₂₄Cl₂N₈Sn 
• 105-07-7 4-cyanobenzaldehyde 
• 155796-90-0 4-(di-1H-pyrrol-2-ylmethyl)benzonitrile 
• 1289037-82-6 (C₆H₄CN)2(C₅H₄N)2SnC₂₀N₄H₈Cl₂ 

Downstream Products

• 1289037-85-9 (C₆H₄CN)2(C₅H₄N)2SnC₂₀N₄H₈(OC₆H₄OCH₃)2 
• 1289037-78-0 (C₆H₄CN)2(C₅H₄N)2SnC₂₀N₄H₈(OC₆H₄O₃(C₂H₄)3NHCO)2C₅H₃N 
• 1310828-40-0 C₇₅H₆₃N₉O₁₀Sn 

Relevant academic research and scientific papers

Open and closed states of a porphyrin based molecular turnstile

The molecular turnstile 1 composed of a stator based on an Sn(iv)-porphyrin bearing two sets of monodentate coordinating sites (pyridyl and benzonitrile) and a handle bearing a 2,6-pyridinediamide moiety as a tridentate unit was synthesised. In the absence of metal behaving as a blocking agent, the handle freely rotates around the stator (open state). In the presence of Pd(ii), the closed state of the turnstile 1-Pd resulting from the simultaneous binding of the metal centre by both the dianionic tridentate site and one of the two pyridyl units is generated. The reaction of 1-Pd with the organometallic 2,6-diphenylpyridine Pt(ii) complex 11 leads to the heterotrinuclear (Pt, Sn, Pd) species 13, resulting from the binding of the platinum complex by 1-Pd. The Royal Society of Chemistry 2011.