Iodination of antipyrine with [N–I–N]+ and carbonyl hypoiodite iodine(i) complexes
| dc.contributor.author | Wilson, Laura M. E. | |
| dc.contributor.author | Rissanen, Kari | |
| dc.contributor.author | Ward, Jas S. | |
| dc.date.accessioned | 2023-02-02T09:43:37Z | |
| dc.date.available | 2023-02-02T09:43:37Z | |
| dc.date.issued | 2023 | |
| dc.identifier.citation | Wilson, L. M. E., Rissanen, K., & Ward, J. S. (2023). Iodination of antipyrine with [N–I–N]+ and carbonyl hypoiodite iodine(i) complexes. <i>New Journal of Chemistry</i>, <i>47</i>(6), 2978-2982. <a href="https://doi.org/10.1039/d2nj05349g" target="_blank">https://doi.org/10.1039/d2nj05349g</a> | |
| dc.identifier.other | CONVID_176419109 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/85298 | |
| dc.description.abstract | A series of iodine(I) complexes, both known and new, were synthesised and the dependence of iodination reactivity on the identity of the Lewis bases and anions present was investigated. Using a previously established screening protocol based on the iodination of antipyrine to iodo-antipyrine, the capability of the iodine(I) species to perform the iodination was tested and compared, especially in relation to Barluenga's reagent, [I(pyridine)2]BF4. The results indicated that the identity of both the Lewis bases and the anion influence the iodination capability of the iodine(I) species, and that the less efficient reagents can deliver favourably comparable percentage conversions with longer reaction times. | en |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | eng | |
| dc.publisher | Royal Society of Chemistry (RSC) | |
| dc.relation.ispartofseries | New Journal of Chemistry | |
| dc.rights | CC BY 4.0 | |
| dc.title | Iodination of antipyrine with [N–I–N]+ and carbonyl hypoiodite iodine(i) complexes | |
| dc.type | research article | |
| dc.identifier.urn | URN:NBN:fi:jyu-202302021580 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Orgaaninen kemia | fi |
| dc.contributor.oppiaine | Organic Chemistry | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 2978-2982 | |
| dc.relation.issn | 1144-0546 | |
| dc.relation.numberinseries | 6 | |
| dc.relation.volume | 47 | |
| dc.type.version | publishedVersion | |
| dc.rights.copyright | © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2023 | |
| dc.rights.accesslevel | openAccess | fi |
| dc.type.publication | article | |
| dc.relation.grantnumber | 351121 | |
| dc.relation.grantnumber | 356187 | |
| dc.subject.yso | karbonyylit | |
| dc.subject.yso | jodi | |
| dc.subject.yso | kemiallinen synteesi | |
| dc.subject.yso | kompleksiyhdisteet | |
| dc.format.content | fulltext | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p14898 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p18902 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p8468 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p30190 | |
| dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
| dc.relation.doi | 10.1039/d2nj05349g | |
| dc.relation.funder | Research Council of Finland | en |
| dc.relation.funder | Research Council of Finland | en |
| dc.relation.funder | Suomen Akatemia | fi |
| dc.relation.funder | Suomen Akatemia | fi |
| jyx.fundingprogram | Academy Project, AoF | en |
| jyx.fundingprogram | Academy Research Fellow, AoF | en |
| jyx.fundingprogram | Akatemiahanke, SA | fi |
| jyx.fundingprogram | Akatemiatutkija, SA | fi |
| jyx.fundinginformation | The authors gratefully acknowledge the Academy of Finland (K. R. grant no. 351121), the Magnus Ehrnrooth Foundation (J. S. W.), and the University of Jyväskylä, Finland for financial support. | |
| dc.type.okm | A1 |
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