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1.
Joykrishna Dey A. Yvette Will Rezik A. Agbaria Peter W. Rabideau Atteye H. Abdourazak Renata Sygula Isiah M. Warner 《Journal of fluorescence》1997,7(3):231-236
The spectroscopic properties of corannulene and cyclopentacorannulene are examined by use of absorption and steady-state fluorescence
measurements. A red shift in the emission maxima of cyclopentacorannulene is noted with respect to the emission maxima in
the corannulene spectrum. Similar differences in the absorption spectra of both molecules are also observed. Reasons for the
dissimilarities in the absorption and emission spectra of these molecules are discussed. The fluorescence quantum yields and
lifetimes of the molecules measured in organic solvents are reported. The fluorescence quantum yield and lifetime of cyclopentacorannulene
are lower than those of corannulene. This difference is attributed to the highly strained and nonplanar structure of cyclopentacorannulene.
The effectiveness of nitromethane as a quencher of corannulene and cyclopentacorannulene fluorescence is examined. In contrast
to previously reported results, the fluorescence of these molecules is quenched by nitromethane. Fluorescence quenching of
the molecules has been attributed to complex formation in the ground state, i.e., static quenching. 相似文献
2.
Martha Mojica Julio A. Alonso Francisco Méndez 《Journal of Physical Organic Chemistry》2013,26(7):526-539
We present a review of the methods most frequently used for the synthesis of fullerenes and the changes that these methods have experienced since 1985 when Kroto and co‐workers discovered C60. We also analyze the most important models that explain the mechanism of the formation of fullerenes in carbon soot, as well as the new methodologies that lead to the rational chemical synthesis of fullerenes and of fullerene fragments as precursors. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
3.
Prof. Richard D. Adams Dr. Poonam Dhull Matthew Pennachio Prof. Marina A. Petrukhina Dr. Mark D. Smith 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(16):4234-4239
The reaction of Re2(CO)8(μ-C6H5)(μ-H), 1 with corannulene (C20H10) yielded the product Re2(CO)8(μ-H)(μ-η2-1,2-C20H9), 2 (65 % yield) containing a Re2 metalated corannulene ligand formed by loss of benzene from 1 and the activation of one of the CH bonds of the nonplanar corannulene molecule by an oxidative-addition to 1 . The corannulenyl ligand has adopted a bridging η2-σ+π coordination to the Re2(CO)8 grouping. Compound 2 reacts with a second equivalent of 1 to yield three isomeric doubly metalated corannulene products: Re2(CO)8(μ-H)(μ-η2-1,2-μ-η2-10,11-C20H8)Re2(CO)8(μ-H), 3 (35 % yield), Re2(CO)8(μ-H)(μ-η2-2,1-μ-η2-10,11-C20H8)Re2(CO)8(μ-H), 4 (12 % yield), and Re2(CO)8(μ-H)(μ-η2-1,2-μ-η2-11,10-C20H8)Re2(CO)8(μ-H), 5 (12 % yield), by a second CH activation on a second rim double bond on the corannulene molecule. The isomers differ by the relative orientations of the coordinated Re2(CO)8(μ-H) groupings. All new products were characterized structurally by single crystal X-ray diffraction analysis. 相似文献
4.
Stack the Bowls: Tailoring the Electronic Structure of Corannulene‐Integrated Crystalline Materials 下载免费PDF全文
Allison M. Rice Ekaterina A. Dolgopolova Brandon J. Yarbrough Gabrielle A. Leith Corey R. Martin Kenneth S. Stephenson Rebecca A. Heugh Amy J. Brandt Prof. Dr. Donna A. Chen Dr. Stavros G. Karakalos Dr. Mark D. Smith Prof. Dr. Kelsey B. Hatzell Dr. Perry J. Pellechia Prof. Dr. Sophya Garashchuk Prof. Dr. Natalia B. Shustova 《Angewandte Chemie (International ed. in English)》2018,57(35):11310-11315
We report the first examples of purely organic donor–acceptor materials with integrated π‐bowls (πBs) that combine not only crystallinity and high surface areas but also exhibit tunable electronic properties, resulting in a four‐orders‐of‐magnitude conductivity enhancement in comparison with the parent framework. In addition to the first report of alkyne–azide cycloaddition utilized for corannulene immobilization in the solid state, we also probed the charge transfer rate within the Marcus theory as a function of mutual πB orientation for the first time, as well as shed light on the density of states near the Fermi edge. These studies could foreshadow new avenues for πB utilization for the development of optoelectronic devices or a route for highly efficient porous electrodes. 相似文献
5.
Hypothetical derivatives of corannulene C20H10 (Cor), namely, CorX5
• radicals, CorX5
− anions (X=H, Cl, or Br), and their η5-π-complexes with SiCp, were calculated by the MNDO/PM3 method. The possibilities of using the results of these calculations
for modeling the electronic structure and geometry of fragments of the analogous complexes of the fullerene derivatives C60X5 are discussed. Calculations of C60X5
• radicals and C60X5
− anions were also carried out. In all the compounds under study, the X atoms are attached to carbon atoms in α positions with
respect to the same five-membered ring.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1268–1272, July, 1997. 相似文献
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Cation-π interactions of curved polycyclic systems: M (M=Li and Na) ion complexation with buckybowls
U.Deva PriyakumarG.Narahari Sastry 《Tetrahedron letters》2003,44(32):6043-6046
B3LYP/6-311+G** calculations on alkali metal ion (Li+ and Na+) complexation with corannulene and sumanene indicate stronger binding compared to [5]-radialene or benzene. The dependence of binding to the convex and concave site is marginal, albeit the preference was consistent for convex binding in the range of 1-4 kcal/mol. The bowl-to-bowl inversion barriers are only marginally affected, below 2 kcal/mol, by metal ion complexation. 相似文献
9.
Cover Picture: Redox‐Active Corannulene Buckybowls in a Crystalline Hybrid Scaffold (Angew. Chem. Int. Ed. 6/2016) 下载免费PDF全文
10.
《Angewandte Chemie (International ed. in English)》2017,56(36):10642-10643