2009
DOI: 10.1007/s00339-008-5014-0
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Purity of rubrene single crystals

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Cited by 33 publications
(31 citation statements)
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“…The three decays are very similar to each other. In particular, the band at 645 nm, which has been argued to grow with oxidation, 6,13,14 decays in the same way as the other bands over multiple time decades. This behavior remained the same among various samples where the prominence of the 645 nm band was different.…”
mentioning
confidence: 95%
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“…The three decays are very similar to each other. In particular, the band at 645 nm, which has been argued to grow with oxidation, 6,13,14 decays in the same way as the other bands over multiple time decades. This behavior remained the same among various samples where the prominence of the 645 nm band was different.…”
mentioning
confidence: 95%
“…6,13 The amplitudes of smaller bands around 645 nm and beyond are more sample dependent and have been partially assigned to oxidation. 6,13,14 We first studied the PL dynamics using 1 ps long pulses obtained from a Light Conversion TOPAS (traveling-wave optical parametric amplifier system) pumped at 1 kHz by a Clark-MXR Ti:sapphire amplifier. We used pulses at a wavelength of 420 nm (absorption length of ∼3 μm) and with an energy of the order of 1 μJ focused to a spot-size of 40 μm on the ab surface of the crystals, paying attention to avoiding any surface imperfections.…”
mentioning
confidence: 99%
“…This re-aromatization , 7). [48,49] Bottom: View along the b axis of the unit cell of 7. The re-aromatization at the former quinone position is reflected by the reduction of the bond length from 4 to 7: 143.8(4) to 139.08 (50) can be achieved by reductive elimination of the peripheral phenyl rings of 7 by using an excess of sodium or potassium.…”
Section: Synthesis Of 56:1112-di-o-phenylenetetracene (Dopt 8) Andmentioning
confidence: 99%
“…This may be a cause for the new strong narrow absorption band at 723 cm −1 , which could be attributed to a twisted Rub conformer CH wagging mode. In the vibrational spectra of peroxides, the characteristic frequency is due to the (O-O) stretching mode, which gives rise to strongly polarized Raman bands about 900-700 cm −1 [23] being, however, weak in the IR absorption. According to [24], the (O-O) stretching vibration interacts with other skeletal C-O and C-C bonds bending vibrations, and there is an extensive coupling between the (O-O), (C-O), and (C-O-O) modes.…”
Section: −C Stretching Vibrations and The Bands At 1589 And 1574 CMmentioning
confidence: 99%