Panchromatic Absorbers Tethered for Bioconjugation or Surface Attachment.

Rui Liu, Jie Rong, Zhiyuan Wu, Masahiko Taniguchi, David F Bocian, Dewey Holten, Jonathan S Lindsey

Abstract 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 1 paper.

0numbers the graph read from it

0cells of the map it votes in

1citing papers in PubMed

–field-weighted citation impact

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

1 citing paper in PubMed.

Porphyrin-Based Compounds: Synthesis and Application.Molecules (Basel, Switzerland) · 2023
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

7 authors.

Rui LiuDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695-8204, USA.ORCID 0000-0003-2927-3080

Jie RongDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695-8204, USA.ORCID 0000-0003-2794-2666

Zhiyuan WuDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695-8204, USA.ORCID 0000-0002-4330-1271

Masahiko TaniguchiDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695-8204, USA.

David F BocianDepartment of Chemistry, University of California, Riverside, CA 92521-0403, USA.

Dewey HoltenDepartment of Chemistry, Washington University, St. Louis, MO 63130-4889, USA.

Jonathan S LindseyDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695-8204, USA.ORCID 0000-0002-4872-2040

Funding

United States Department of Energy DE-FG02-05ER15661

6 · The paper itself

Abstract

The syntheses of two triads are reported. Each triad is composed of two perylene-monoimides linked to a porphyrin via an ethyne unit, which bridges the perylene 9-position and a porphyrin 5- or 15-position. Each triad also contains a single tether composed of an alkynoic acid or an isophthalate unit. Each triad provides panchromatic absorption (350-700 nm) with fluorescence emission in the near-infrared region (733 or 743 nm; fluorescence quantum yield ~0.2). The syntheses rely on the preparation of

Indexed as

PerylenePorphyrinsPerylenePorphyrinsarrayartificial photosynthesisbuilding blockcopper-free Sonogashira couplingethyneperyleneporphyrinsolar

Identifiers

PMID36235037

DOI10.3390/molecules27196501

PMCPMC9573448

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.