1281983-36-5

Upstream product

• 1281983-33-2 F₂B((C₄H₂NCl)2(CC₆H₃(C(CH₃)3)2)) 
• 181762-72-1 (3,5-di-tert-butylphenyl)di(pyrrol-2-yl)methane 
• 81353-38-0 (trimethylsilylethynyl)tributyltin 

Downstream Products

• 1281983-39-8 [F₂B(C₄H₂NCC)2(CC(3,5-di-tert-butylphenyl))]2 
• 1281983-42-3 [F₂B(C₄H₂NCC)2(CC(3,5-di-tert-butylphenyl))]3 

Relevant academic research and scientific papers

Metal-mediated synthesis of antiaromatic porphyrinoids from a BODIPY precursor

(Figure Presented) Metallic route to antiaromaticity: The synthesis of a butadiyne-bridged cyclic BODIPY dimer (see structure; C white, B orange, N blue, F green) and trimer was achieved through Pd-catalyzed Stille coupling and Cu-mediated Glaser-type coupling. These cyclic BODIPYs were found to be stable 24π- and 36π-antiaromatic porphyrinoids with planar conformations, and their structures, electronic states, and reactivity were explored.