2009
DOI: 10.1016/j.jphotochem.2008.12.020
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Synthesis and properties of novel chemiluminescent biological probes: 2- and 3-(2-Succinimidyloxycarbonylethyl)phenyl acridinium esters

Abstract: This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their pe… Show more

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Cited by 19 publications
(42 citation statements)
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“…Relatively high contribution of H···F and F···H interactions (9.8%), disclosed for 3, presumably results from the occurrence of disordered anionic fragment (CF 3 OSO 2 − ), in which the oxygen atoms may exchange with the fluorine ones. 1 H and 13 C NMR spectra recorded for compounds 1, 2 and 3 disclose a similar pattern, observed for previously investigated symmetric ACA derivaƟves (Figs S2 †, S3 †). 55 The most deshielded protons, located in the spatial proximity of the nitrogen or oxygen atoms (H1/H8 and H4/H5, respecƟvely (Fig.…”
Section: The Hirshfeld Surfacessupporting
confidence: 85%
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“…Relatively high contribution of H···F and F···H interactions (9.8%), disclosed for 3, presumably results from the occurrence of disordered anionic fragment (CF 3 OSO 2 − ), in which the oxygen atoms may exchange with the fluorine ones. 1 H and 13 C NMR spectra recorded for compounds 1, 2 and 3 disclose a similar pattern, observed for previously investigated symmetric ACA derivaƟves (Figs S2 †, S3 †). 55 The most deshielded protons, located in the spatial proximity of the nitrogen or oxygen atoms (H1/H8 and H4/H5, respecƟvely (Fig.…”
Section: The Hirshfeld Surfacessupporting
confidence: 85%
“…29 A complementary two-dimensional mappings are also presented, which summarize quantitatively the types of intermolecular contacts experienced by chemical entities in the bulk. 1 Table S1 † and selected spectra are presented in Figs S1 † and S2 †. The mass spectra of 1−3 were recorded employing Biflex III MALDI-TOF mass spectrometer, working in the positive polarity mode with the 150-600 m/z range of scan and the attenuation of the laser beam set at 60%.…”
Section: Hirshfeld Surface Analysismentioning
confidence: 99%
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“…41 A solution of salicyl alcohol (23 mmol) in 95:5 1,2-dichloroethane:methanol was cooled on ice for 30 min. Br2 (19 mmol) in dichloromethane was added dropwise to the solution and the mixture was stirred for 2 h at 0 C. The resulting solution was washed with water until a neutral aqueous phase is obtained, and then evaporated.…”
Section: Reagents and Chemicalsmentioning
confidence: 99%