Wednesday, March 28, 2012

Synthesis and Properties of [9]Cyclo-1,4-naphthylene: A π-Extended Carbon Nanoring

Akiko Yagi, Yasutomo Segawa, and Kenichiro Itami Journal of the America Chemical Society 2012, 134, 2962–2965 (Paywall)
Contributed by Steven Bachrach.
Reposted from Computational Organic Chemistry with permission

Itami continues to design novel macrocycles containing aromatic rings (see this post). This latest paper reports the synthesis of the first nanohoops containing naphthylenes, namely [9]cyclo-1,4-naphthylene 1. Since the macrocycle contains an odd number of naphthylene units, the lowest energy conformation is of C2 symmetry with one of the naphthylene rings in the plane of the macrocycle. This conformation gives rise to 27 peaks in the proton NMR, and while the value of the computed chemical shifts differ from the experimental ones by about 0.5 to 1 ppm, their relative ordering is in very nice agreement.

Itami also notes that 1 is chiral and computed the barrier for racemization of 19.9 kcal mol-1¸ through the transition state 2. This racemization process is compared with the racemization of 1,1’-binaphthyl.

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