<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao M</submitter><funding>the Scientific Research and Innovation Fund Project of Shandong Energy Research Institute</funding><funding>Guangxi Science and Technology Project</funding><funding>Linyi University</funding><funding>Taishan Scholars Program of Shandong Province</funding><pagination>3612</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9459928</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(17)</volume><pubmed_abstract>Iron complexes of the types [Fe(HL)&lt;sub>2&lt;/sub>Cl&lt;sub>2&lt;/sub>] (&lt;b>Fe1&lt;/b>: HL&lt;sup>1&lt;/sup> = pyridine-2-aldoxime; &lt;b>Fe2&lt;/b>: HL&lt;sup>2&lt;/sup> = 6-methylpyridine-2-aldoxime; &lt;b>Fe3&lt;/b>: HL&lt;sup>3&lt;/sup> = phenyl-2-pyridylketoxime; &lt;b>Fe4&lt;/b>: HL&lt;sup>4&lt;/sup> = picolinaldehyde O-methyl oxime) were prepared and characterized by elemental analysis and IR spectroscopy. The crystal structure of &lt;b>Fe2&lt;/b>, determined by single-crystal X-ray diffraction, featured a distorted octahedral coordination of the iron center binding with two ligands of HL&lt;sup>2&lt;/sup>. The X-ray structure and infrared spectral data indicated that pyridine-oxime ligands act as unionized bidentate ligand by coordinating with N&lt;sub>pyridine&lt;/sub> and N&lt;sub>oxime&lt;/sub>. The catalytic performance for isoprene polymerization, catal</pubmed_abstract><journal>Polymers</journal><pubmed_title>Synthesis, Characterization and Catalytic Property Studies for Isoprene Polymerization of Iron Complexes Bearing Unionized Pyridine-Oxime Ligands.</pubmed_title><pmcid>PMC9459928</pmcid><funding_grant_id>SEI S202101</funding_grant_id><funding_grant_id>LYDX2020BS012</funding_grant_id><funding_grant_id>tsqn201812112</funding_grant_id><funding_grant_id>Grant No. AB21196038；Talent No. AD21238015</funding_grant_id><pubmed_authors>Zhao M</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Zhu G</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis, Characterization and Catalytic Property Studies for Isoprene Polymerization of Iron Complexes Bearing Unionized Pyridine-Oxime Ligands.</name><description>Iron complexes of the types [Fe(HL)&lt;sub>2&lt;/sub>Cl&lt;sub>2&lt;/sub>] (&lt;b>Fe1&lt;/b>: HL&lt;sup>1&lt;/sup> = pyridine-2-aldoxime; &lt;b>Fe2&lt;/b>: HL&lt;sup>2&lt;/sup> = 6-methylpyridine-2-aldoxime; &lt;b>Fe3&lt;/b>: HL&lt;sup>3&lt;/sup> = phenyl-2-pyridylketoxime; &lt;b>Fe4&lt;/b>: HL&lt;sup>4&lt;/sup> = picolinaldehyde O-methyl oxime) were prepared and characterized by elemental analysis and IR spectroscopy. The crystal structure of &lt;b>Fe2&lt;/b>, determined by single-crystal X-ray diffraction, featured a distorted octahedral coordination of the iron center binding with two ligands of HL&lt;sup>2&lt;/sup>. The X-ray structure and infrared spectral data indicated that pyridine-oxime ligands act as unionized bidentate ligand by coordinating with N&lt;sub>pyridine&lt;/sub> and N&lt;sub>oxime&lt;/sub>. The catalytic performance for isoprene polymerization, catal</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-19T07:09:08.014Z</modification><creation>2025-04-19T07:09:08.014Z</creation></dates><accession>S-EPMC9459928</accession><cross_references><pubmed>36080685</pubmed><doi>10.3390/polym14173612</doi></cross_references></HashMap>