The DOI matches its Crossref record.
para-Bridged Symmetrical Pillar[5]arenes: Their Lewis Acid Catalyzed Synthesis and Host–Guest Property
Abstract
Condensation of 1,4-dimethoxybenzene (DMB) with paraformaldehyde in the presence of BF3.O(C2H5)2 gave novel para-bridged pentacyclic pillar DMB (DMpillar[5]arene). Moreover, para-bridged pentacyclic hydroquinone (pillar[5]arene) was prepared. Pillar[5]arene formed 1:1 host-guest complexes with dialkyl viologen and alkyl pyridinium derivatives. However, pillar[5]arene did not form complexes with the diadamantyl viologen derivative since a bulky adamantyl group was unable to thread the cavity of pillar[5]arene.
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.
Integrity signals
Registry
Cites
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.
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
Cited by
Metal–Organic Framework (MOF)‐Based Drug/Cargo Delivery and Cancer Therapy
Wu, M., & Yang, Y. (2017) · Advanced Materials · doi:10.1002/adma.201606134 · Cited by 2,285
Pillararenes, A New Class of Macrocycles for Supramolecular Chemistry
Xue, M., Yang, Y., Chi, X., Zhang, Z., & Huang, F. (2012) · Accounts of Chemical Research · doi:10.1021/ar2003418 · Cited by 1,449
Surveying macrocyclic chemistry: from flexible crown ethers to rigid cyclophanes
Liu, Z., Nalluri, S. K. M., & Stoddart, J. F. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00185a · Cited by 909
Metal–Organic Framework‐Based Stimuli‐Responsive Systems for Drug Delivery
Cai, W., Wang, J., Chu, C., Chen, W., Wu, C., & Liu, G. (2019) · Advanced Science · doi:10.1002/advs.201801526 · Cited by 744
Xia, D., Wang, P., Ji, X., Khashab, N. M., Sessler, J. L., & Huang, F. (2020) · Chemical Reviews · doi:10.1021/acs.chemrev.9b00839 · Cited by 734
Zhang, Z., Luo, Y., Chen, J., Dong, S., Yu, Y., Ma, Z., & Huang, F. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201006693 · Cited by 720
Zhou, J., Yu, G., & Huang, F. (2017) · Chemical Society Reviews · doi:10.1039/c6cs00898d · Cited by 677
Experimental Binding Energies in Supramolecular Complexes
Biedermann, F., & Schneider, H.-J. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00583 · Cited by 554
Li, Z.-Y., Zhang, Y., Zhang, C.-W., Chen, L.-J., Wang, C., Tan, H., Yu, Y., Li, X., & Yang, H.-B. (2014) · Journal of the American Chemical Society · doi:10.1021/ja413047r · Cited by 537
Nonporous Adaptive Crystals of Pillararenes
Jie, K., Zhou, Y., Li, E., & Huang, F. (2018) · Accounts of Chemical Research · doi:10.1021/acs.accounts.8b00255 · Cited by 533
Pillar[5]arenes: fascinating cyclophanes with a bright future
Cragg, P. J., & Sharma, K. (2012) · Chem. Soc. Rev. · doi:10.1039/c1cs15164a · Cited by 531
Monofunctionalized Pillar[5]arene as a Host for Alkanediamines
Strutt, N. L., Forgan, R. S., Spruell, J. M., Botros, Y. Y., & Stoddart, J. F. (2011) · Journal of the American Chemical Society · doi:10.1021/ja111418j · Cited by 507
Yu, G., Zhou, X., Zhang, Z., Han, C., Mao, Z., Gao, C., & Huang, F. (2012) · Journal of the American Chemical Society · doi:10.1021/ja3099905 · Cited by 486
Ligands for f-element extraction used in the nuclear fuel cycle
Leoncini, A., Huskens, J., & Verboom, W. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00574a · Cited by 486
Pillar[6]arene-Based Photoresponsive Host–Guest Complexation
Yu, G., Han, C., Zhang, Z., Chen, J., Yan, X., Zheng, B., Liu, S., & Huang, F. (2012) · Journal of the American Chemical Society · doi:10.1021/ja302998q · Cited by 481
Diverse gatekeepers for mesoporous silica nanoparticle based drug delivery systems
Wen, J., Yang, K., Liu, F., Li, H., Xu, Y., & Sun, S. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00219j · Cited by 477
Lee, S., Chen, C.-H., & Flood, A. H. (2013) · Nature Chemistry · doi:10.1038/nchem.1668 · Cited by 443
Yu, G., Xue, M., Zhang, Z., Li, J., Han, C., & Huang, F. (2012) · Journal of the American Chemical Society · doi:10.1021/ja306399f · Cited by 431
Chang, Y., Yang, K., Wei, P., Huang, S., Pei, Y., Zhao, W., & Pei, Z. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201407272 · Cited by 366
Chiral Selective Transmembrane Transport of Amino Acids through Artificial Channels
Chen, L., Si, W., Zhang, L., Tang, G., Li, Z.-T., & Hou, J.-L. (2013) · Journal of the American Chemical Society · doi:10.1021/ja312704e · Cited by 305
Wang, Y., Ping, G., & Li, C. (2016) · Chemical Communications · doi:10.1039/c6cc03999e · Cited by 293
1,8-Naphthalimide-based fluorescent chemosensors: recent advances and perspectives
Dong, H.-Q., Wei, T.-B., Ma, X.-Q., Yang, Q.-Y., Zhang, Y.-F., Sun, Y.-J., Shi, B.-B., Yao, H., Zhang, Y.-M., & Lin, Q. (2020) · Journal of Materials Chemistry C · doi:10.1039/d0tc03681a · Cited by 285
Complex interactions of pillar[5]arene with paraquats and bis(pyridinium) derivatives
Li, C., Xu, Q., Li, J., Yao, F., & Jia, X. (2010) · Organic & Biomolecular Chemistry · doi:10.1039/b920146g · Cited by 279
Vapochromic crystals: understanding vapochromism from the perspective of crystal engineering
Li, E., Jie, K., Liu, M., Sheng, X., Zhu, W., & Huang, F. (2020) · Chemical Society Reviews · doi:10.1039/c9cs00098d · Cited by 267
Near-Ideal Xylene Selectivity in Adaptive Molecular Pillar[n]arene Crystals
Jie, K., Liu, M., Zhou, Y., Little, M. A., Pulido, A., Chong, S. Y., Stephenson, A., Hughes, A. R., Sakakibara, F., Ogoshi, T., et al. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b02621 · Cited by 258
Self-citationEfficient Aggregation‐Induced Emission Manipulated by Polymer Host Materials
Wang, X., Song, N., Hou, W., Wang, C., Wang, Y., Tang, J., & Yang, Y. (2019) · Advanced Materials · doi:10.1002/adma.201903962 · Cited by 185
Metadata
- Authors
- Ogoshi, T., Kanai, S., Fujinami, S., Yamagishi, T.-A., & Nakamoto, Y.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2008-03-22
- Volume
- 130
- Issue
- 15
- Pages
- 5022-5023
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2088252867
- Cited by
- 2,200
- References
- 0
- FWCI
- 9.08
- 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
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.
