Synthesis, supramolecular insight, Hirshfeld surface analyses and optical properties of Fe(II) and Cu(II) complexes of flexible imidazole tethered 1,8-naphthalimide
{"title":"Synthesis, supramolecular insight, Hirshfeld surface analyses and optical properties of Fe(II) and Cu(II) complexes of flexible imidazole tethered 1,8-naphthalimide","authors":"Jayanta Kr. Nath","doi":"10.1007/s11243-024-00572-z","DOIUrl":null,"url":null,"abstract":"<div><p>Two mononuclear complexes of transition metal {Fe(II) and Cu(II)} constructed from <i>2-(3-(1H-imidazol-1-yl)propyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione</i> (<b>L</b>)and KSCN as auxiliary ligand are reported. Both the complexes were formed in refluxed condition. The complexes were characterized with different spectroscopic tools such as FT-IR, UV–vis, CHN-elemental analysis, photoluminescence. The solid-state structures were determined by single crystal X-ray diffraction method which exhibit that Fe (II) center, in complex 1, is four coordinated distorted tetrahedral geometry whereas Cu(II) center, in complex 2 is five coordinated square pyramidal geometry with slight distortion. The bulk stability was confirmed by powder XRD data. The thermal stability of both complexes was determined by thermogravimetric analysis (TGA). Various types of supramolecular interactions such as O–H…O, C–H…O, <i>π</i>…<i>π</i>, C–H…π and C–H…S were observed in the x-ray structures, and all these interactions guide the formation of 3D supramolecular architecture in the solid-state of both complexes. Besides these, the 2D-fingerprint (2D-FP) and Hirshfeld surface analysis (HSA) computations were served to prove the 2D-network packed crystal lattice interactions.</p></div>","PeriodicalId":803,"journal":{"name":"Transition Metal Chemistry","volume":"49 3","pages":"171 - 181"},"PeriodicalIF":1.6000,"publicationDate":"2024-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transition Metal Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11243-024-00572-z","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Two mononuclear complexes of transition metal {Fe(II) and Cu(II)} constructed from 2-(3-(1H-imidazol-1-yl)propyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione (L)and KSCN as auxiliary ligand are reported. Both the complexes were formed in refluxed condition. The complexes were characterized with different spectroscopic tools such as FT-IR, UV–vis, CHN-elemental analysis, photoluminescence. The solid-state structures were determined by single crystal X-ray diffraction method which exhibit that Fe (II) center, in complex 1, is four coordinated distorted tetrahedral geometry whereas Cu(II) center, in complex 2 is five coordinated square pyramidal geometry with slight distortion. The bulk stability was confirmed by powder XRD data. The thermal stability of both complexes was determined by thermogravimetric analysis (TGA). Various types of supramolecular interactions such as O–H…O, C–H…O, π…π, C–H…π and C–H…S were observed in the x-ray structures, and all these interactions guide the formation of 3D supramolecular architecture in the solid-state of both complexes. Besides these, the 2D-fingerprint (2D-FP) and Hirshfeld surface analysis (HSA) computations were served to prove the 2D-network packed crystal lattice interactions.
期刊介绍:
Transition Metal Chemistry is an international journal designed to deal with all aspects of the subject embodied in the title: the preparation of transition metal-based molecular compounds of all kinds (including complexes of the Group 12 elements), their structural, physical, kinetic, catalytic and biological properties, their use in chemical synthesis as well as their application in the widest context, their role in naturally occurring systems etc.
Manuscripts submitted to the journal should be of broad appeal to the readership and for this reason, papers which are confined to more specialised studies such as the measurement of solution phase equilibria or thermal decomposition studies, or papers which include extensive material on f-block elements, or papers dealing with non-molecular materials, will not normally be considered for publication. Work describing new ligands or coordination geometries must provide sufficient evidence for the confident assignment of structural formulae; this will usually take the form of one or more X-ray crystal structures.