2001
DOI: 10.1016/s1386-1425(01)00457-7
|View full text |Cite
|
Sign up to set email alerts
|

Evolution of absorption, fluorescence, laser and chemical properties in the series of compounds perylene, benzo(ghi)perylene and coronene

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

6
44
0

Year Published

2003
2003
2021
2021

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 59 publications
(50 citation statements)
references
References 12 publications
6
44
0
Order By: Relevance
“…Note that the discharge is switched off when the clusters are ionized by the laser. The laser wavelength of 308 nm is very close to the strong S 0 −→ S β transition of neutral coronene (Nijegorodov et al 2001). Upon absorbing several photons, the coronene is electronically excited and ionized.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Note that the discharge is switched off when the clusters are ionized by the laser. The laser wavelength of 308 nm is very close to the strong S 0 −→ S β transition of neutral coronene (Nijegorodov et al 2001). Upon absorbing several photons, the coronene is electronically excited and ionized.…”
Section: Methodsmentioning
confidence: 99%
“…The discharge in the cluster source is switched off, so that only cold neutral coronene clusters enter the first acceleration zone of the RETOF. Thanks to the presence of strong absorption bands in both neutral coronene (Nijegorodov et al 2001) and its cation (Shida 1988) in this energy range, multiple sequential absorption of several photons is expected to occur within the cluster during the laser pulse (typical duration 10 ns). Only two photons are needed to overpass the IP of the coronene monomer, i.e.…”
Section: Photoinduced Productsmentioning
confidence: 99%
“…All dehydro [5]helicene (or naphthoperylene) derivatives showed good solubility in common organic solvents, such as Figure 3, the UV/Vis spectrum of dehydro [5]helicene 10 a in cyclohexane exhibited the maximum absorption band at 436 nm, a bathochromic shift of 51 nm compared to benzoA C H T U N G T R E N N U N G [g,h,i]perylene, [21] which is probably due to the larger conjugated p system and the electron-donating effect of methoxy groups in 10 a. In the fluorescent spectrum, the maximum emission wavelength of 10 a was observed at 478 nm, which was consistent with cyan fluorescence.…”
mentioning
confidence: 99%
“…the dipole moment of which is directed parallel to the long axis of the molecule [27e29]. Two other absorption bands, one parallel (S 0 / S b ) and one perpendicular (S 0 / S a ) to the molecular long axis, are observed for perylene and its derivatives in UV region [28,29] and were not recorded in our experiment. The position of the maxima and the shape of the band in the visible region do not depend on the substituents.…”
Section: Surface Pressureemean Molecular Area Isothermmentioning
confidence: 76%