Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 505

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Incorporation of Imidazolium-Based Poly(ionic liquid)s into a Metal–Organic Framework for CO2 Capture and Conversion

Ding, Meili, Jiang, Hai-Long·2018·ACS Catalysis

Abstract

The rational integration of multiple functional components into a composite material could result in enhanced activity tailored for specific applications. Herein, imidazolium-based poly(ionic liquid)s (denoted as polyILs) have been confined into the metal–organic framework (MOF) material MIL-101 via in situ polymerization of encapsulated monomers. The resultant composite polyILs@MIL-101 exhibits good CO 2 capture capability that is beneficial for the catalysis of the cycloaddition of CO 2 with epoxides to form cyclic carbonates at subatmospheric pressure in the absence of any cocatalyst. The significantly enhanced activity of polyILs@MIL-101, compared to either MIL-101 or polyILs, is attributed to the synergistic effect among the good CO 2 enrichment capacity, the Lewis acid sites in the MOF, as well as the Lewis base sites in the polyILs.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1021/acscatal.7b03404

Cites

3 of 3 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 3 references

Cited by

See all 505

Metadata

Authors
Ding, M., & Jiang, H.-L.
Venue
ACS Catalysis
Published
2018-03-08
Volume
8
Issue
4
Pages
3194-3201
ISSN
2155-5435 (ISSN-L)
OpenAlex
W2790798973
Cited by
505
References
3
FWCI
16.96
Type
journal article
Language
en
Open access
closed

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Incorporation of Imidazolium-Based Poly(ionic liquid)s into a Metal–Organic Framework for CO2 Capture and Conversion. https://app.cochat.ai/papers/10.1021/acscatal.7b03404
The paper
Ding, M., & Jiang, H.-L. (2018). Incorporation of Imidazolium-Based Poly(ionic liquid)s into a Metal–Organic Framework for CO2 Capture and Conversion. ACS Catalysis. https://doi.org/10.1021/acscatal.7b03404

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.