Evidence map›Paper›PMID 35684394›Full record

ArticleMolecules (Basel, Switzerland)2022

Data-Driven and Multiscale Modeling of DNA-Templated Dye Aggregates.

Austin Biaggne, Lawrence Spear, German Barcenas, Maia Ketteridge, Young C Kim, Joseph S Melinger, William B Knowlton, Bernard Yurke, Lan Li

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Tunable Electronic Structure via DNA-Templated Heteroaggregates of Two Distinct Cyanine Dyes.The journal of physical chemistry. C, Nanomaterials and interfaces · 2022
    Article
  5. 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

9 authors at 2 institutions in 1 country.

Austin BiaggneMicron School of Materials Science and Engineering, Boise State University, Boise, ID 83725, USA.ORCID 0000-0003-2807-4960
Lawrence SpearMicron School of Materials Science and Engineering, Boise State University, Boise, ID 83725, USA.
German BarcenasMicron School of Materials Science and Engineering, Boise State University, Boise, ID 83725, USA.ORCID 0000-0002-9936-7720
Maia KetteridgeMicron School of Materials Science and Engineering, Boise State University, Boise, ID 83725, USA.
Young C KimMaterials Science and Technology Division, U.S. Naval Research Laboratory, Washington, DC 20375, USA.
Joseph S MelingerElectronics Science and Technology Division, U.S. Naval Research Laboratory, Washington, DC 20375, USA.
William B KnowltonMicron School of Materials Science and Engineering, Boise State University, Boise, ID 83725, USA.
Bernard YurkeMicron School of Materials Science and Engineering, Boise State University, Boise, ID 83725, USA.
Lan LiMicron School of Materials Science and Engineering, Boise State University, Boise, ID 83725, USA.ORCID 0000-0003-3870-8437
Micron (United States) · USUnited States Naval Research Laboratory · US

Funding

Department of the Navy, Office of Naval Research (ONR) N00014-19-1-2615U.S. Department of Energy (DoE), Office of Basic Energy Sciences, Division of Materials Science and Engineering through the Established Program to Stimulate Competitive Research (EPSCoR) DE-SC0020089
6 · The paper itself

Abstract

Dye aggregates are of interest for excitonic applications, including biomedical imaging, organic photovoltaics, and quantum information systems. Dyes with large transition dipole moments (μ) are necessary to optimize coupling within dye aggregates. Extinction coefficients (ε) can be used to determine the μ of dyes, and so dyes with a large ε (>150,000 M−1cm−1) should be engineered or identified. However, dye properties leading to a large ε are not fully understood, and low-throughput methods of dye screening, such as experimental measurements or density functional theory (DFT) calculations, can be time-consuming. In order to screen large datasets of molecules for desirable properties (i.e., large ε and μ), a computational workflow was established using machine learning (ML), DFT, time-dependent (TD-) DFT, and molecular dynamics (MD). ML models were developed through training and validation on a dataset of 8802 dyes using structural features. A Classifier was developed with an accuracy of 97% and a Regressor was constructed with an R2 of above 0.9, comparing between experiment and ML prediction. Using the Regressor, the ε values of over 18,000 dyes were predicted. The top 100 dyes were further screened using DFT and TD-DFT to identify 15 dyes with a μ relative to a reference dye, pentamethine indocyanine dye Cy5. Two benchmark MD simulations were performed on Cy5 and Cy5.5 dimers, and it was found that MD could accurately capture experimental results. The results of this study exhibit that our computational workflow for identifying dyes with a large μ for excitonic applications is effective and can be used as a tool to develop new dyes for excitonic applications.

Indexed as

Coloring AgentsMolecular Dynamics SimulationDNADNA ReplicationColoring AgentsDNAdensity functional theoryDNA scaffoldsdye aggregatesexcitonextinction coefficientmachine learningmolecular dynamicstime-dependent density functional theorytransition dipole moment

Identifiers

PMID35684394
PMCPMC9182218
OpenAlexW4281747656

What OpenQuestion holds

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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.