To Fold or to Assemble?

Wang, Wei; Li, Linsong; Helms, Greg; Zhou, Hanhan; Li, Alexander D. Q.

doi:10.1021/ja027186h

Cited by 229 publications

(191 citation statements)

References 20 publications

Supporting

Mentioning

172

Contrasting

Order By: Relevance

“…The formation of this new band in the emission spectrum of PBIs has been extensively discussed in the literature. According to Wang et al 35,[76][77][78] who examined the self-organization of a PEG functionalized PBI in chloroform solution, such a red shifted band in the emission spectrum of PBIs may be attributed to the fluorescence properties of molecular assemblies of increased size. The same conclusions have also been outlined by Neuteboom and coworkers 79 when studying the optical features of polytetrahydrofuran substituted PBI polymers in ODCB.…”

Section: Resultsmentioning

confidence: 99%

Novel EDTA-ligands containing an integral perylene bisimide (PBI) core as an optical reporter unit

et al. 2014

View full text Add to dashboard Cite

The synthesis, characterization and metal complexation of a new class of perylene bisimides (PBIs) as an integral part of ethylenediaminetetraacetic acid (EDTA) are reported. The simplest representative, namely derivative 1a, was synthesized both by a convergent as well as a direct approach while the elongated derivatives, 1b and 1c, were obtained only via a convergent synthetic pathway. All these new prototypes of water-soluble perylenes are bolaamphiphiles and were fully characterized by 1 H-and 13 C-NMR spectroscopy, matrix assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry and IR spectroscopy. In order to acquaint ourselves with the behaviour in solution of our PBIs bearing dendritic wedges, the simplest derivative, 1a, was chosen and tested by means of UV/Vis and fluorescence spectroscopy as well as by zeta-potential measurements. A photoexcitation induced intramolecular photo-electron transfer (PET) can be observed in these molecules. Therefore their potential applications as sensors can be imagined. Model compound 1a efficiently coordinates trivalent metal cations both in water and dimethyl sulfoxide (DMSO). Significantly, the effects of the complexation strongly depend on the aggregation state of the PBI molecules in solution. As a matter of fact, in water, the presence of M 3+ ions triggers the formation of light emitting supramolecular aggregates (excimers). On the other hand, in DMSO-rich solutions metal complexation leads to the suppression of the PET and leads to a strong fluorescence enhancement.

show abstract

Section: Resultsmentioning

confidence: 99%

Novel EDTA-ligands containing an integral perylene bisimide (PBI) core as an optical reporter unit

et al. 2014

View full text Add to dashboard Cite

show abstract

“…Hence, the strong intermolecular vibrational-electronic coupling in PDI derivatives has been well studied. 6,[16][17][18][19][20][21] The formation of PDI assemblies leads to broad vibrational-electronic coupling due to fused aromatic rings whose molecular orbital overlap with adjacent neighbors. In contrast, free PDI derivatives provide clear vibrational-electronic coupling.…”

Section: Resultsmentioning

confidence: 99%

“…[1][2][3][4] Perylene diimides (PDIs) derivatives effectively form supramolecular assemblies through p-p stacking interaction. [5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21] In particular, supramolecular assemblies based on calixarenePDI conjugates show efficient energy and electron transfer properties due to the well-defined rigid and electron-rich scaffolds of calixarenes. [22][23][24][25][26][27] We have prepared PDI derivatives with a high emission property in aqueous solutions.…”

Section: Introductionmentioning

confidence: 99%

Emission properties of cyclodextrin dimers linked with perylene diimide—effect of cyclodextrin tumbling

Takashima

Otsubo

et al. 2012

Polym J

View full text Add to dashboard Cite

Perylene diimide (PDI) derivatives with cyclodextrins (PDI-CD 2 s) exhibit specific emission properties, which depend on the type of CDs in an aqueous solution. Herein we successfully create an emission film-kneaded PDI-CD 2 derivatives via effective tumbling of the altropyranose unit. PDI-6CD 2 s are crosslinked with PDI between 6-amino-CDs. Although the emission intensities of PDI-6CD 2 s in dimethyl sulfoxide are similar regardless of the type of CD, PDI-6cCD 2 has a relatively high emission intensity in aqueous solutions. In contrast, for PDIC 7 -3CD 2 s, which are linked with N,N'-bis(6-carboxylhexyl)perylene-3,4,9,10-tetracarboxyl diimide (BisC 7 -PDI) between 3-amino-CDs, the emission intensity of PDIC 7 -3bCD 2 is stronger than those of PDIC 7 -3aCD 2 , PDIC 7 -3cCD 2 , and PDI-6CD 2 s in aqueous solutions. The selective emission behavior of PDIC 7 -3CD 2 s is due to the formation of the pseudo[1]rotaxane dimer through tumbling of the altropyranose unit in an aqueous solution. PDIC 7 -3bCD 2 in the solid state does not demonstrate a distinctive emission due to self-quenching, whereas PDIC 7 -3bCD 2 kneaded into the polyvinyl alcohol (PVA) film exhibits a bright yellow emission. The order of the emission intensities of PDIC 7 -3CD 2 s kneaded into PVA films is similar to those in aqueous solutions. INTRODUCTIONRecently, supramolecular assemblies with extended aromatic compounds have attracted much attention. 1-4 Perylene diimides (PDIs) derivatives effectively form supramolecular assemblies through p-p stacking interaction. [5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21] In particular, supramolecular assemblies based on calixarenePDI conjugates show efficient energy and electron transfer properties due to the well-defined rigid and electron-rich scaffolds of calixarenes. [22][23][24][25][26][27] We have prepared PDI derivatives with a high emission property in aqueous solutions.Generally, PDI derivatives have low solubilities in aqueous solutions. Even if PDI derivatives are dissolved in aqueous solutions by introducing a hydrophilic group, the emission of PDI derivatives exhibit self-quenching in aqueous solutions due to the formation of supramolecular assemblies and folders. To create water-soluble and effective emission sensor materials with PDI derivatives, we have introduced CDs into the PDI motif. The CDs are a family of macrocyclic oligosaccharides; the most common are composed of 6 (a), 7 (b), or 8 (g) a-1,4-linked D-glucopyranose units. [28][29][30][31][32][33][34] The introduction of CDs should influence the molecular recognition property and increase the emission intensity. Although supramolecular assemblies based on permethylated CDPDI conjugates have been previously reported, 35-38 the formation of assemblies cannot prevent the decrease in the monomer emission intensity of the PDI units due

show abstract

“…These three molecules were deposited on ITO using the SA method and their properties were compared along with those of the SA PDI-phenyl-PA. PDI aggregation causes broadening of the visible absorbance bands and can be assessed by the relative intensity of the 0-0 and 0-1 vibronic bands, with a 0-0/0-1 band ratio close to 1.6 considered to be monomeric. 34 Although the ATR UV-vis spectra (Fig. 6) shows that aggregation exists in all four films, the degree varied.…”

Section: ·2 Perylene Diimide Modifiersmentioning

confidence: 94%

Characterization of Charge-Transfer Kinetics at Organic/Electrode Interfaces Using Potential-modulated Attenuated Total Reflectance (PM-ATR) Spectroscopy

Zheng

Saavedra

2017

ANAL. SCI.

View full text Add to dashboard Cite

To Fold or to Assemble?

Cited by 229 publications

References 20 publications

Novel EDTA-ligands containing an integral perylene bisimide (PBI) core as an optical reporter unit

Novel EDTA-ligands containing an integral perylene bisimide (PBI) core as an optical reporter unit

Emission properties of cyclodextrin dimers linked with perylene diimide—effect of cyclodextrin tumbling

Characterization of Charge-Transfer Kinetics at Organic/Electrode Interfaces Using Potential-modulated Attenuated Total Reflectance (PM-ATR) Spectroscopy

Contact Info

Product

Resources

About