Evidence map›Paper›PMID 35638322›Full record

ArticleAngewandte Chemie (International ed. in English)2022

Intramolecular Energy and Solvent-Dependent Chirality Transfer within a BINOL-Perylene Hetero-Cyclophane.

Guanghui Ouyang, Jessica Rühe, Yang Zhang, Mei-Jin Lin, Minghua Liu, Frank Würthner

Open access · hybridAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
7.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. A Bis-Perylene Diimide Macrocycle Chiroptical Switch.Angewandte Chemie (International ed. in English) · 2025
    Article
  8. Control of Dynamic Chirality in Donor-Acceptor Fluorophores.Angewandte Chemie (International ed. in English) · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Guanghui OuyangUniversität Würzburg, Institut für Organische Chemie & Center for Nanosystems Chemistry, Am Hubland, 97074, Würzburg, Germany.ORCID http://orcid.org/0000-0002-9605-2723
Jessica RüheUniversität Würzburg, Institut für Organische Chemie & Center for Nanosystems Chemistry, Am Hubland, 97074, Würzburg, Germany.ORCID http://orcid.org/0000-0001-6595-1112
Yang ZhangState Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, 350116, Fuzhou, China.
Mei-Jin LinState Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, 350116, Fuzhou, China.ORCID http://orcid.org/0000-0003-2008-9674
Minghua LiuCAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, ZhongGuanCun, North First Street 2, 100190, Beijing, China.ORCID http://orcid.org/0000-0002-6603-1251
Frank WürthnerUniversität Würzburg, Institut für Organische Chemie & Center for Nanosystems Chemistry, Am Hubland, 97074, Würzburg, Germany.ORCID http://orcid.org/0000-0001-7245-0471
Chinese Academy of Sciences · CNFuzhou University · CN

Funding

Chinese Academy of Sciences 2019036Stiftung Begabtenförderung Cusanuswerk
6 · The paper itself

Abstract

Multichromophoric macrocycles and cyclophanes are important supramolecular architectures for the elucidation of interchromophoric interactions originating from precise spatial organization. Herein, by combining an axially chiral binaphthol bisimide (BBI) and a bay-substituted conformationally labile twisted perylene bisimide (PBI) within a cyclophane of well-defined geometry, we report a chiral PBI hetero-cyclophane (BBI-PBI) that shows intramolecular energy and solvent-regulated chirality transfer from the BBI to the PBI subunit. Excellent spectral overlap and spatial arrangement of BBI and PBI lead to efficient excitation energy transfer and subsequent PBI emission with high quantum yield (80-98 %) in various solvents. In contrast, chirality transfer is strongly dependent on the respective solvent as revealed by circular dichroism (CD) spectroscopy. The combination of energy and chirality transfer affords a bright red circularly polarized luminescence (CPL) from the PBI chromophore by excitation of BBI.

Indexed as

Chirality TransferCyclophanesEnergy TransferPerylene BisimideSolvent Effects

Identifiers

PMID35638322
PMCPMC9400993
OpenAlexW4281673050

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.