42052-40-4

Upstream product

• 3355-29-1 1,1-dimethyl-3-phenylprop-2-ynyl chloride 
• 536-74-3 phenylacetylene 
• 6738-06-3 phenylethynylmagnesium bromide 
• 13941-57-6 4-(tert-butyl(dimethyl)silanyl)-2-methyl-3-butyn-2-ol 
• 591-50-4 iodobenzene 
• 1422189-19-2 3,3,-dimethyl-1-(tert-butyl(dimethyl)silyl)-5-trimethylsilyl-1,4-pentadiyne 
• 1719-19-3 2-Methyl-4-phenyl-3-butyn-2-ol 

Downstream Products

• 42052-41-5 (3,3-dimethyl-5-phenylcyclopenta-1,4-dien-1-yl)benzene 
• 42052-42-6 cis-3,3-imethyl-1,5-diphenyl-1-penten-4-yn 
• 1313031-92-3 C₁₉H₂₀N₂ 
• 1055230-48-2 2-benzylidene-3,3-dimethyl-5-phenyl-3,4-dihydro-2H-pyrrole 
• 1055230-50-6 4,4-dimethyl-2,6-diphenyl-3,4-dihydropyridine 
• 177995-56-1 C₁₉H₁₆I₂ 

Relevant academic research and scientific papers

Unraveling factors leading to efficient norbornadiene-quadricyclane molecular solar-thermal energy storage systems

Developing norbornadiene-quadricyclane (NBD-QC) systems for molecular solar-thermal (MOST) energy storage is often a process of trial and error. By studying a series of norbornadienes (NBD-R2) doubly substituted at the C7-position with R = H, M

Cross-hyperconjugation: An unexplored orbital interaction between π-conjugated and saturated molecular segments

Crossing a barrier: Molecules with saturated ER2 units (E=C or Si, R=electron-releasing group) inserted between two π-conjugated segments have electronic and optical properties that resemble those of cross-conjugated molecules (see figure). This cross-hyperconjugation provides a deeper understanding of the conjugation phenomenon, and is an alternative to cross-conjugation in the design of molecules for nano and materials applications. Copyright