𝔖 Bobbio Scriptorium

✦ LIBER ✦

Comment on “New Assignment of the Electronically Excited States of Anthracene-9,10-endoperoxide and Its Derivatives: A Critical Experimental and Theoretical Study”

✍ Scribed by Brauer, Hans-Dieter; Schmidt, Reinhard

Book ID: 120034999
Publisher: American Chemical Society
Year: 2000
Tongue: English
Weight: 22 KB
Volume: 104
Category: Article
ISSN: 1089-5639
DOI: 10.1021/jp992840+

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reply to the Comment on “New Assignment

Reply to the Comment on “New Assignment of the Electronically Excited States of Anthracene-9,10-endoperoxide and Its Derivatives: A Critical Experimental and Theoretical Study”

✍ Gudipati, Murthy S.; Klein, Andreas 📂 Article 📅 2000 🏛 American Chemical Society 🌐 English ⚖ 19 KB

New Assignment of the Electronically Exc

New Assignment of the Electronically Excited States of Anthracene-9,10-endoperoxide and Its Derivatives: A Critical Experimental and Theoretical Study †

✍ Klein, Andreas; Kalb, Martin; Gudipati, Murthy S. 📂 Article 📅 1999 🏛 American Chemical Society 🌐 English ⚖ 183 KB

A Theoretical Study on Electronically Ex

A Theoretical Study on Electronically Excited States of the Hydrogen-Bonded Clusters for Fluorenone and Fluorenone Derivatives in Methanol Solvent

✍ Yufei Cheng, Xiaoyu Zhang, Weiping Zhang 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 542 KB

Electrophilic and oxidative chemistry of

Electrophilic and oxidative chemistry of pyrene and its non-alternant isomers: theoretical (DFT, GIAO-NMR, NICS) study of protonation carbocations and oxidation dications from pyrene, azupyrene (dicyclopenta[ef,kl]heptalene) and dicyclohepta[ed,gh]pentaleneElectronic supplementary information (ESI) available: Table S1: Electronic energies (E), zero point energies (ZPE) and Gibbs free energies (G) obtained from DFT calculations for the studied molecules and cations at B3LYP/6-31G(d) level. Figs. S1, S8 and S10 and Tables S2?S14: Optimized structures and Cartesian coordinates for 1, 1aH+, 1bH22+, 12+, 2, 2aH+, 2aH22+, 22+, 3, 3cH+, 3eH22+ and 32+. Figs. S2, S3 and S4: Computed 13C NMR chemical shifts and NPA-derived charges for 1aH+, 122+ and 12+. Fig. S5: Experimental 13C NMR chemical shifts for 1aH+ and 12+. Figs. S6, S7, and S12: HOMO?LUMO forms in the oxidation dications. Figs. S9 and S11: Bond-lengths in X-ray derived and computed structures for 2 and 3. See http://www.rsc.org/suppdata/ob/b4/b405009f/

✍ Okazaki, Takao; Laali, Kenneth K. 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 409 KB