Evidence map›Paper›PMID 32313237›Full record

ArticleNature chemistry2020

Enantioselective photoinduced cyclodimerization of a prochiral anthracene derivative adsorbed on helical metal nanostructures.

Xueqin Wei, Junjun Liu, Guang-Jie Xia, Junhong Deng, Peng Sun, Jason J Chruma, Wanhua Wu, Cheng Yang, Yang-Gang Wang, Zhifeng Huang

Abstract read
PubMed Publisher
In one paragraph

Article in Nature chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed, 145 citations in OpenAlex.

  1. Article
  2. Can nanozymes achieve more than enzymes?Nature reviews. Materials · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Plasmonic Chirality Meets Reactivity: Challenges and Opportunities.The journal of physical chemistry. C, Nanomaterials and interfaces · 2025
    Review
  9. Review
  10. Review
  11. Article
  12. Seed-Mediated Growth and Advanced Characterization of Chiral Gold Nanorods.Advanced materials (Deerfield Beach, Fla.) · 2024
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

10 authors at 4 institutions in 2 countries.

Xueqin Wei *Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, State Key Laboratory of Biotherapy, and Healthy Food Evaluation Research Center, Sichuan University, Chengdu, China.
Junjun Liu *Department of Physics, Institute of Advanced Materials, State Key Laboratory of Environmental and Biological Analysis, Golden Meditech Centre for NeuroRegeneration Sciences, Hong Kong Baptist University (HKBU), Hong Kong SAR, China.
Guang-Jie Xia *Department of Chemistry and Guandong Provincial Key Laboratory of Catalytic Chemistry, Southern University of Science and Technology (SUSTech), Shenzhen, China.ORCID http://orcid.org/0000-0002-4892-6289
Junhong DengDepartment of Materials Science and Engineering, SUSTech, Shenzhen, China.
Peng SunDepartment of Physics, Institute of Advanced Materials, State Key Laboratory of Environmental and Biological Analysis, Golden Meditech Centre for NeuroRegeneration Sciences, Hong Kong Baptist University (HKBU), Hong Kong SAR, China.
Jason J ChrumaKey Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, State Key Laboratory of Biotherapy, and Healthy Food Evaluation Research Center, Sichuan University, Chengdu, China.ORCID http://orcid.org/0000-0002-3669-4863
Wanhua WuKey Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, State Key Laboratory of Biotherapy, and Healthy Food Evaluation Research Center, Sichuan University, Chengdu, China.ORCID http://orcid.org/0000-0002-8969-1148
Cheng YangKey Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, State Key Laboratory of Biotherapy, and Healthy Food Evaluation Research Center, Sichuan University, Chengdu, China. yangchengyc@scu.edu.cn.ORCID http://orcid.org/0000-0002-2049-1324
Yang-Gang WangDepartment of Chemistry and Guandong Provincial Key Laboratory of Catalytic Chemistry, Southern University of Science and Technology (SUSTech), Shenzhen, China. wangyg@sustech.edu.cn.ORCID http://orcid.org/0000-0002-0582-0855
Zhifeng HuangDepartment of Physics, Institute of Advanced Materials, State Key Laboratory of Environmental and Biological Analysis, Golden Meditech Centre for NeuroRegeneration Sciences, Hong Kong Baptist University (HKBU), Hong Kong SAR, China. zfhuang@hkbu.edu.hk.ORCID http://orcid.org/0000-0002-9613-9423
Hong Kong Baptist University · HKSichuan University · CNSouthern University of Science and Technology · CNGuangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The generation of molecular chirality in the absence of any molecular chiral inductor is challenging and of fundamental interest for developing a better understanding of homochirality. Here, we show the manipulation of molecular chirality through control of the handedness of helical metal nanostructures (referred to as nanohelices) that are produced by glancing angle deposition onto a substrate that rotates in either a clockwise or counterclockwise direction. A prochiral molecule, 2-anthracenecarboxylic acid, is stereoselectively adsorbed on the metal nanohelices as enantiomorphous anti-head-to-head dimers. The dimers show either Si-Si or Re-Re facial stacking depending on the handedness of the nanohelices, which results in a specific enantiopreference during their photoinduced cyclodimerization: a left-handed nanohelix leads to the formation of (+)-cyclodimers, whereas a right-handed one gives (-)-cyclodimers. Density functional theory calculations, in good agreement with the experimental results, point to the enantioselectivity mainly arising from the selective spatial matching of either Si-Si or Re-Re facial stacking at the helical surface; it may also be influenced by chiroplasmonic effects.

Identifiers

PMID32313237
OpenAlexW3016534225

What OpenQuestion holds

Textmetadata
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.