Reference health

Silver Clusters as Robust Nodes and π–<i>A</i>ctivation Sites for the Construction of Heterogeneous Catalysts for the Cycloaddition of Propargylamines

https://doi.org/10.1021/acscatal.7b02844
CiteStamped reference-health badge
75/75 checkable references clean · checked 2026-07-23

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

3 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 75 checked references that resolve
resolves10.1038/531180a
Putting carbon dioxide to work
resolves10.1126/science.291.5501.48
Toward Sustainable Chemistry
resolves10.1246/cl.2009.786
Silver-catalyzed Preparation of Oxazolidinones from Carbon Dioxide and Propargylic Amines
resolves10.1039/C5CS00895F
Silver-catalyzed carboxylation
resolves10.1039/C5GC02311D
Efficient conversion of carbon dioxide at atmospheric pressure to 2-oxazolidinones promoted by bifunctional Cu( <scp>ii</scp> )-substituted polyoxometalate-based ionic liquids
resolves10.1002/cssc.201601469
In Situ Generated Zinc(II) Catalyst for Incorporation of CO<sub>2</sub> into 2‐Oxazolidinones with Propargylic Amines at Atmospheric Pressure
resolves10.1002/ajoc.201600114
A Carboxylative Cyclization of Propargylic Amines with Carbon Dioxide Catalyzed by the N‐Heterocyclic Carbene 1,3‐Di‐<i>tert</i>‐butylimidazol‐2‐ylidene (ItBu)
resolves10.1021/acssuschemeng.6b01288
New Copper(I)/DBU Catalyst System for the Carboxylative Cyclization of Propargylic Amines with Atmospheric CO<sub>2</sub>: An Experimental and Theoretical Study
resolves10.1021/acscatal.5b01335
Mechanistic Aspects of the Carboxylative Cyclization of Propargylamines and Carbon Dioxide Catalyzed by Gold(I) Complexes Bearing an<i>N</i>-Heterocyclic Carbene Ligand
resolves10.1021/acscatal.7b00209
Valorization of CO<sub>2</sub>: Preparation of 2-Oxazolidinones by Metal–Ligand Cooperative Catalysis with SCS Indenediide Pd Complexes
resolves10.1021/cr030110z
Streptogramins, Oxazolidinones, and Other Inhibitors of Bacterial Protein Synthesis
resolves10.1016/j.tetasy.2003.12.015
Chiral auxiliaries in polymer-supported organic synthesis
resolves10.1021/cr030024z
Synthetic Preparation of <i>N</i>-Methyl-α-amino Acids
resolves10.1038/465691a
Lessons in carbon trading
resolves10.1016/j.apenergy.2015.07.067
Methanol synthesis using captured CO2 as raw material: Techno-economic and environmental assessment
resolves10.1126/science.aaa8075
Function-led design of new porous materials
resolves10.1039/C4CS00103F
Metal–organic frameworks for artificial photosynthesis and photocatalysis
resolves10.1126/science.aaf2458
Pore chemistry and size control in hybrid porous materials for acetylene capture from ethylene
resolves10.1021/jacs.5b10491
An Adsorbate Discriminatory Gate Effect in a Flexible Porous Coordination Polymer for Selective Adsorption of CO<sub>2</sub> over C<sub>2</sub>H<sub>2</sub>
resolves10.1021/ar1000617
Rational Design, Synthesis, Purification, and Activation of Metal−Organic Framework Materials
resolves10.1126/science.1230444
The Chemistry and Applications of Metal-Organic Frameworks
resolves10.1002/cssc.201700748
Greening the Processes of Metal–Organic Framework Synthesis and their Use in Sustainable Catalysis
resolves10.1021/acs.chemrev.7b00091
Metal–Organic Frameworks for Heterogeneous Basic Catalysis
resolves10.1002/anie.201511484
Inserting CO<sub>2</sub> into Aryl C−H Bonds of Metal–Organic Frameworks: CO<sub>2</sub> Utilization for Direct Heterogeneous C−H Activation
resolves10.1002/smll.201602711
Metal‐Organic Frameworks for CO<sub>2</sub> Chemical Transformations
resolves10.1002/anie.201409103
An Efficient Nanoscale Heterogeneous Catalyst for the Capture and Conversion of Carbon Dioxide at Ambient Pressure
resolves10.1002/anie.201603934
Tuning Pore Size in Square‐Lattice Coordination Networks for Size‐Selective Sieving of CO<sub>2</sub>
resolves10.1021/cr400392k
Topological Analysis of Metal–Organic Frameworks with Polytopic Linkers and/or Multiple Building Units and the Minimal Transitivity Principle
resolves10.1039/C4CS00003J
Tuning the structure and function of metal–organic frameworks via linker design
resolves10.1021/cr200205j
Deconstructing the Crystal Structures of Metal–Organic Frameworks and Related Materials into Their Underlying Nets
resolves10.1021/acs.inorgchem.7b01685
A Polyoxovanadate–Resorcin[4]arene-Based Porous Metal–Organic Framework as an Efficient Multifunctional Catalyst for the Cycloaddition of CO<sub>2</sub> with Epoxides and the Selective Oxidation of Sulfides
resolves10.1021/acsami.7b03835
Porous MOF with Highly Efficient Selectivity and Chemical Conversion for CO<sub>2</sub>
resolves10.1002/chem.201504747
A Versatile Cu<sup>II</sup> Metal–Organic Framework Exhibiting High Gas Storage Capacity with Selectivity for CO<sub>2</sub>: Conversion of CO<sub>2</sub> to Cyclic Carbonate and Other Catalytic Abilities
resolves10.1016/j.apcatb.2017.07.085
Pentanuclear Yb(III) cluster-based metal-organic frameworks as heterogeneous catalysts for CO2 conversion
resolves10.1021/jacs.5b07925
Metal–Organic Polymers Containing Discrete Single-Walled Nanotube as a Heterogeneous Catalyst for the Cycloaddition of Carbon Dioxide to Epoxides
resolves10.1002/anie.201309778
Crystal Engineering of an nbo Topology Metal–Organic Framework for Chemical Fixation of CO<sub>2</sub> under Ambient Conditions
resolves10.1039/C7CC01136A
Cluster-based MOFs with accelerated chemical conversion of CO <sub>2</sub> through C–C bond formation
resolves10.1039/C6CC05845K
A microporous Cu-MOF with optimized open metal sites and pore spaces for high gas storage and active chemical fixation of CO <sub>2</sub>
resolves10.1021/jacs.5b13335
A Triazole-Containing Metal–Organic Framework as a Highly Effective and Substrate Size-Dependent Catalyst for CO<sub>2</sub> Conversion
resolves10.1039/C5CC07781H
A sustainable protocol for the facile synthesis of zinc-glutamate MOF: an efficient catalyst for room temperature CO <sub>2</sub> fixation reactions under wet conditions
resolves10.1002/ejic.201600218
Anionic Metal–Organic Framework for Selective Dye Removal and CO<sub>2</sub> Fixation
resolves10.1039/C5TA07026K
Bifunctional MOF heterogeneous catalysts based on the synergy of dual functional sites for efficient conversion of CO <sub>2</sub> under mild and co-catalyst free conditions
resolves10.1039/C4CC09410G
Investigation of prototypal MOFs consisting of polyhedral cages with accessible Lewis-acid sites for quinoline synthesis
resolves10.1021/ja508626n
A Hafnium-Based Metal–Organic Framework as an Efficient and Multifunctional Catalyst for Facile CO<sub>2</sub> Fixation and Regioselective and Enantioretentive Epoxide Activation
resolves10.1021/ja502119z
Introduction of π-Complexation into Porous Aromatic Framework for Highly Selective Adsorption of Ethylene over Ethane
resolves10.1021/acscatal.6b03404
Alkyne Activation by a Porous Silver Coordination Polymer for Heterogeneous Catalysis of Carbon Dioxide Cycloaddition
resolves10.3762/bjoc.10.46
Silver and gold-catalyzed multicomponent reactions
resolves10.1002/ejoc.200700169
Silver‐Catalyzed Incorporation of Carbon Dioxide into Propargylic Alcohols
resolves10.1038/nature11990
X-ray analysis on the nanogram to microgram scale using porous complexes
resolves10.1126/science.aaf9135
Coordinative alignment of molecules in chiral metal-organic frameworks
resolves10.1021/jacs.6b05706
A Mesoporous Indium Metal–Organic Framework: Remarkable Advances in Catalytic Activity for Strecker Reaction of Ketones
resolves10.1038/nature14327
Cooperative insertion of CO2 in diamine-appended metal-organic frameworks
resolves10.1016/j.inoche.2011.09.045
A trinuclear silver coordination polymer from a bipyridine bis-urea macrocyclic ligand and silver triflate
resolves10.1021/ic970694l
Crystal Structure, Electronic Structure, and Temperature-Dependent Raman Spectra of Tl[Ag(CN)<sub>2</sub>]:  Evidence for Ligand-Unsupported Argentophilic Interactions
resolves10.1107/S0021889802022112
Single-crystal structure validation with the program<i>PLATON</i>
resolves10.1002/adsc.201500639
Robust Silver(I) Catalyst for the Carboxylative Cyclization of Propargylic Alcohols with Carbon Dioxide under Ambient Conditions
resolves10.1021/ja2051149
Understanding the Preferential Adsorption of CO<sub>2</sub> over N<sub>2</sub> in a Flexible Metal–Organic Framework
resolves10.1016/S0924-2031(02)00099-1
Vibrational and electronic studies on some metal thiourea complexes
resolves10.1038/ncomms10007
Polyoxometalate-based homochiral metal-organic frameworks for tandem asymmetric transformation of cyclic carbonates from olefins
resolves10.1039/C4NR07103D
Degradable polyphosphoester-based silver-loaded nanoparticles as therapeutics for bacterial lung infections
resolves10.1039/c0cc05331g
Carbon-bonded silver nanoparticles: alkyne-functionalized ligands for SERS imaging of mammalian cells
resolves10.1016/j.vibspec.2009.04.008
Adsorption change of cyclohexyl acetylene on gold nanoparticle surfaces
resolves10.1016/j.vibspec.2006.04.006
Concentration dependent Raman study of 1,4-diethynylbenzene on gold nanoparticle surfaces
resolves10.1021/ja904232v
Monomeric Copper(I), Silver(I), and Gold(I) Alkyne Complexes and the Coinage Metal Family Group Trends
resolves10.1063/1.458452
An all-electron numerical method for solving the local density functional for polyatomic molecules
resolves10.1063/1.1316015
From molecules to solids with the DMol3 approach
resolves10.1103/PhysRevLett.77.3865
Generalized Gradient Approximation Made Simple
resolves10.1103/PhysRevB.66.155125
Hardness conserving semilocal pseudopotentials
resolves10.1103/PhysRevB.80.205414
Azobenzene at coinage metal surfaces: Role of dispersive van der Waals interactions
resolves10.1103/PhysRevB.13.5188
Special points for Brillouin-zone integrations
resolves10.1007/BF00549096
Bonded-atom fragments for describing molecular charge densities
resolves10.1038/srep10876
Pd loaded amphiphilic COF as catalyst for multi-fold Heck reactions, C-C couplings and CO oxidation
resolves10.1021/am9006897
Novel Low Band Gap Small Molecule and Phenylenevinylene Copolymer with Cyanovinylene 4-Nitrophenyl Segments: Synthesis and Application for Efficient Bulk Heterojunction Solar Cells
resolves10.1039/C6CC01171C
Highly crystalline covalent organic frameworks from flexible building blocks
resolves10.1002/chem.201402365
Triazine‐Based Mesoporous Covalent Imine Polymers as Solid Supports for Copper‐Mediated Chan–Lam Cross‐Coupling N‐Arylation Reactions
The 3 references without a DOI — listed, not checked
no DOI — not checkedSMART Data collection software (version 5.629);Bruker AXS Inc.,Madison, WI, 2003.
no DOI — not checkedSAINT Data reduction software (version 6.45);Bruker AXS Inc.,Madison, WI, 2003.
no DOI — not checkedSheldrick, G. M.SHELXTL97 Program for crystal structure solution;University of Göttingen,Göttingen, Germany, 1997.
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

checked 2026-07-23 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record

Embed this badge

Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.

<a href="https://citestamp.com/citestamped/10.1021/acscatal.7b02844"><img src="https://citestamp.com/citestamped/10.1021/acscatal.7b02844/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[![CiteStamped reference-health badge](https://citestamp.com/citestamped/10.1021/acscatal.7b02844/badge.svg)](https://citestamp.com/citestamped/10.1021/acscatal.7b02844)