Infrared and Raman spectra of thin solid films of 1,2-bis(propylimido perylene) ethane

Rodriguez-Llorente, S.; Aroca, Ricardo F.; Duff, J. W.

doi:10.1016/s1386-1425(98)00238-8

Cited by 30 publications

(25 citation statements)

References 20 publications

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“…5. In line with that of perylene analogous [59][60][61], the principal in-plane bands at 1660 and 1698 cm −1 correspond to the O=CN stretches while the in-plane bands at 1596 and 1572 cm −1 correspond to the C=C aromatic stretches. The principal out-of-plane band is at 812 cm −1 and has been assigned as the wagging modes of C-H on perylene ring.…”

Section: Ft-ir Spectrasupporting

confidence: 68%

Supramolecular self-assembly study of a flexible perylenetetracarboxylic diimide dimer in Langmuir and Langmuir–Blodgett films

Chen

Kong

Wang

et al. 2009

Journal of Colloid and Interface Science

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Section: Ft-ir Spectrasupporting

confidence: 68%

Supramolecular self-assembly study of a flexible perylenetetracarboxylic diimide dimer in Langmuir and Langmuir–Blodgett films

Chen

Kong

Wang

et al. 2009

Journal of Colloid and Interface Science

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“…It should be underscored that in the range from 300 nm to 400 nm, the absorption spectra were multiplied by a factor of 300 to enhance the readability. The vibrational progression of the electronic states, characteristics of all PTCDs, exhibits peaks separated by 170 meV; such progression is often described by an effective internal vibrational mode of the perylene moiety [17,27,28]. In the region of the twophoton absorption measurements, i.e.…”

Section: Methodsmentioning

confidence: 99%

Two-photon absorption of perylene derivatives: Interpreting the spectral structure

Piovesan

Silva

Boni

et al. 2009

Chemical Physics Letters

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a b s t r a c tThis work investigates the two-photon absorption spectrum of perylene tetracarboxylic derivatives using the white-light continuum Z-scan technique. Perylene derivatives present relatively high two-photon absorption cross-section, which makes them attractive for applications in photonics. Because of the spectral resolution of the white-light continuum Z-scan, we were able to observe a well defined structure in the two-photon absorption spectrum, composed by two distinct peaks. These peaks, as well as the resonant enhancement of the nonlinearity, were modeled using the sum-over-states approach considering a four-level energy diagram with two final two-photon states. The existence of such states was confirmed using the response function formalism within the DFT framework.

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“…The compounds were synthetized according to two methods settled on the basis of literature data [12][13][14][15][16][17]. Specifically, the new protocols proposed have allowed us to isolate the perylene monoimides easily and with good yields conversely to what we have obtained by following exclusively the literature synthetic pathways.…”

Section: Resultsmentioning

confidence: 99%

Synthesis of Alternative Electron Acceptor Compounds

Troisi¹,

Citti²,

Granito³

et al. 2015

TOOCJ

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New perylene monoimides, diimides and bis-diimides have been designed and synthetized. A detailed investigation of the synthesis of these compounds has also been performed in order to highlight the crucial factors for obtaining a specific class of molecules. Specifically, the attention has been focused on the synthesis of the intermediate perylene monoimides which are very useful precursors for many molecules difficult to obtain. Furthemore, two synthetic pathways have been developed for obtaining the bis-diimides variously substituted. These final compounds are predicted to mimic the excellent electron acceptor properties of fullerene derivatives and they can be used as building blocks to form 3D semiconducting materials.

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Infrared and Raman spectra of thin solid films of 1,2-bis(propylimido perylene) ethane

Cited by 30 publications

References 20 publications

Supramolecular self-assembly study of a flexible perylenetetracarboxylic diimide dimer in Langmuir and Langmuir–Blodgett films

Supramolecular self-assembly study of a flexible perylenetetracarboxylic diimide dimer in Langmuir and Langmuir–Blodgett films

Two-photon absorption of perylene derivatives: Interpreting the spectral structure

Synthesis of Alternative Electron Acceptor Compounds

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