Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Lesya Kobryn"'
Autor:
Marina A. Petrukhina, Yulia Sevryugina, Lesya Kobryn, Renata Sygula, Sarah N. Spisak, Alexander V. Zabula, Andrzej Sygula
Publikováno v:
Chem. Commun.. 50:2657-2659
The X-ray crystallographic study of C60H28 consisting of two tethered corannulene bowls revealed a unique solid-state packing based on tight convex-concave π-π interactions. The controlled reduction of C60H28 resulted in the isolation and structura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79c1761ecdd1a667b53d8ef568594dcf
https://doi.org/10.1039/c3cc49451a
https://doi.org/10.1039/c3cc49451a
Publikováno v:
Fragments of Fullerenes and Carbon Nanotubes: Designed Synthesis, Unusual Reactions, and Coordination Chemistry
Application of the synthetic methodology developed in our laboratory yields molecular clips and tweezers with corannulene pincers and cyclooctadiene or cyclooctatetraene tethers. These highly nonplanar systems possess a potential for binding guest mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::764cd36b086dfb8c075e54e9534e1fee
https://doi.org/10.1016/j.tetlet.2009.09.177
https://doi.org/10.1016/j.tetlet.2009.09.177
Publikováno v:
Dyes and Pigments. 63:203-211
One of the main problems in expanding the application of the coumarin derivatives is a search of new ways for deeping the color and increasing the intensity of the spectral bands. A series of 6-derivatives of 2H-2-chromenone were synthesized. The UV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::576706ca48dd124e46a0692feb28e3c3
https://doi.org/10.1016/j.dyepig.2004.02.008
https://doi.org/10.1016/j.dyepig.2004.02.008
Publikováno v:
Organic Letters. 10:3927-3929
2-Trimethylsilylcorannulenyl trifluoromethanesulfonate, prepared from bromocorannulene, provides a means for generating of 1,2-didehydrocorannulene (corannulyne) under very mild conditions as demonstrated by the high-yield formation of its adducts wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c92b50b0d857051ea2e9d24c20f872
https://doi.org/10.1021/ol801581z
https://doi.org/10.1021/ol801581z
Publikováno v:
Physical chemistry chemical physics : PCCP. 12(26)
The dispersion corrected B97-D functional studies find a previously overlooked conformer of the buckycatcher C(60)H(28) (2) exhibiting intramolecular pi-pi stacking of its corannulene pincers to represent a global potential energy minimum conformatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b87f2c03a84d04676450086dd1667406
https://pubmed.ncbi.nlm.nih.gov/20517563
https://pubmed.ncbi.nlm.nih.gov/20517563
Publikováno v:
Proceedings of The 12th International Electronic Conference on Synthetic Organic Chemistry.
The presence of opposite by sOH shifts of ortho-protons (downfield, if the substitution takes place in ?-position and upper-field – in ?-position) by the substitution of hydrogen atoms for methyl groups in alkyl chain of alkylbenzenes has been foun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b4d6115774ab91fad629b7ca9080045
https://doi.org/10.3390/ecsoc-12-01232
https://doi.org/10.3390/ecsoc-12-01232
Publikováno v:
Proceedings of The 8th International Electronic Conference on Synthetic Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65fb3c2bdf9162d700cc63c365dfc4ec
https://doi.org/10.3390/ecsoc-8-01940
https://doi.org/10.3390/ecsoc-8-01940
Publikováno v:
Organic Letters; Aug2008, Vol. 10 Issue 17, p3927-3929, 3p
The nature of electronic transitions in coumarin, 3-arylcoumarins and their sulfur-containing analog
Publikováno v:
ResearcherID
Scopus-Elsevier
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0fb28cb0b052a52070c10b578aaf632f
http://www.scopus.com/inward/record.url?eid=2-s2.0-12244286799&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-12244286799&partnerID=MN8TOARS
