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2-吡啶基金属茂,第九部分。硫取代的2-吡啶基二茂铁:合成及其对Pt(II)和Hg(II)的反应活性

2-Pyridylmetallocenes, Part IX. Sulphur-Substituted 2-Pyridylferrocene: Synthesis and Reactivity towards Pt(II) and Hg(II).

作者信息

Weigand Stefan, Sünkel Karlheinz

机构信息

Department of Chemistry, Ludwig-Maximilians University Munich, 81377 Munich, Germany.

出版信息

Molecules. 2024 Oct 15;29(20):4884. doi: 10.3390/molecules29204884.

DOI:10.3390/molecules29204884
PMID:39459252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11510587/
Abstract

Thio-substituted 2-pyridylferrocenes [CpFe{CH(X)(CHN)}] (X = SOTol, ; SMe, ) were prepared from [CpFe(CHR)] (R = SOTol, ; 2-CHN, ) in moderate yields. The reactions of and with [PtCl(DMSO)] yielded the binuclear N, S chelated complexes [CpFe{CH(X)(CHN)}-(к-N,S)-PtCl] (X= SOTol, , SMe, ), while the reaction of with Hg(OAc)/LiCl led to cyclomercuration with generation of [CpFe{CH(SMe)(CHN)(HgCl)}], . The crystal structures of ·CHCl and were determined. The structure of showed a weak intramolecular Fe…Pt interaction and several weak intermolecular interactions involving all Cl atoms. Weak intermolecular interactions between Hg and S atoms in the cyclomercurated led to a tetrameric structure involving a HgS ring.

摘要

硫代取代的2-吡啶基二茂铁[CpFe{CH(X)(CHN)}](X = SOTol, ;SMe, )由[CpFe(CHR)](R = SOTol, ;2-CHN, )以中等产率制备。 和 与[PtCl(DMSO)]的反应生成了双核N,S螯合配合物[CpFe{CH(X)(CHN)}-(к-N,S)-PtCl](X = SOTol, ,SMe, ),而 与Hg(OAc)/LiCl的反应导致环汞化,生成[CpFe{CH(SMe)(CHN)(HgCl)}], 。测定了 ·CHCl和 的晶体结构。 的结构显示出弱的分子内Fe…Pt相互作用以及涉及所有Cl原子的几个弱分子间相互作用。环汞化产物中Hg和S原子之间的弱分子间相互作用导致形成包含HgS环的四聚体结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/d1168a205df4/molecules-29-04884-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/fd97df8b96cd/molecules-29-04884-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/bb3d786ea401/molecules-29-04884-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/ab1171575b79/molecules-29-04884-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/0d0ee9228096/molecules-29-04884-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/42efd74a2f33/molecules-29-04884-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/b30901da465a/molecules-29-04884-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/645a590ce410/molecules-29-04884-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/046a0fcba056/molecules-29-04884-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/d1168a205df4/molecules-29-04884-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/fd97df8b96cd/molecules-29-04884-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/bb3d786ea401/molecules-29-04884-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/ab1171575b79/molecules-29-04884-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/0d0ee9228096/molecules-29-04884-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/42efd74a2f33/molecules-29-04884-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/b30901da465a/molecules-29-04884-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/645a590ce410/molecules-29-04884-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/046a0fcba056/molecules-29-04884-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11510587/d1168a205df4/molecules-29-04884-g006.jpg

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