Chiral Sum Frequency Spectroscopy of Thin Films of Porphyrin J-Aggregates

2009 ◽  
Vol 113 (15) ◽  
pp. 5098-5103 ◽  
Author(s):  
Tetsuhiko Nagahara ◽  
Kenji Kisoda ◽  
Hiroshi Harima ◽  
Misako Aida ◽  
Taka-aki Ishibashi
2014 ◽  
Vol 615 ◽  
pp. 124-131 ◽  
Author(s):  
Jean-Sebastién Samson ◽  
Rüdiger Scheu ◽  
Nikolay Smolentsev ◽  
Steven W. Rick ◽  
Sylvie Roke

1998 ◽  
Author(s):  
Roman V. Markov ◽  
Alexander I. Plekhanov ◽  
Sergei G. Rautian ◽  
Natalja A. Orlova ◽  
Vladimir V. Shelkovnikov ◽  
...  

2018 ◽  
Vol 122 (46) ◽  
pp. 9031-9042 ◽  
Author(s):  
Jonathan D. Handali ◽  
Kyle F. Sunden ◽  
Blaise J. Thompson ◽  
Nathan A. Neff-Mallon ◽  
Emily M. Kaufman ◽  
...  

2014 ◽  
Vol 2 (1) ◽  
Author(s):  
Rebecca Flamini ◽  
Benedetta Carlotti ◽  
Anna Spalletti ◽  
Assunta Marrocchi

AbstractWe report the photobehaviour of a series of eight structurally related arylacetylene derivatives, in solution as well as in pristine and PC61BM blended thin-_lms. The formation of both H- and J-aggregates in the solid state have been demonstrated, and, interestingly, an energy transfer from H-aggregates or/and from residual "unstacked" molecules to J-aggregates has been found, the latter being the only emitting species. The fuorescence quenching by PC61BM at di_erent loadings has been studied in blend films, and it has been found particularly effcient in the case of a symmetrical peripheral substitution of the acetylene derivative core. Preliminary time-resolved measurements in emission (ns resolution) and in absorption (fs resolution) con_rmed the H⟶J energy transfer and underlined the presence of delayed fuorescence from Jaggregates, formed by energy transfer from the long-lived first excited singlet state of H-aggregates. In all cases, a homogeneous surface morphology of thin films.


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