<?xml version="1.0"?>
<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Magnetic interactions in coordination species with 5-sulfosalicylates</dc:title><dc:creator>Kozlevčar,	Bojan	(Avtor)
	</dc:creator><dc:creator>Jagličić,	Zvonko	(Avtor)
	</dc:creator><dc:creator>Pevec,	Andrej	(Avtor)
	</dc:creator><dc:subject>5-sulfosalicylic acid</dc:subject><dc:subject>copper</dc:subject><dc:subject>cobalt</dc:subject><dc:subject>structure</dc:subject><dc:subject>antiferromagnetism</dc:subject><dc:description>5-sulfosalicylic acid (H$_3$L) poses three potential coordination groups (carboxylic, sulfonic and hydroxylic) that can deprotonate and enable versatile coordination options with metal ions. This includes a bridging mode, a suitable way to enable stronger magnetic interactions, among adjacent metal ions. Several novel coordination compounds with 5-sulfosalicylates were synthesized and characterized. These are {[Cu(inia)(HL)(H$_2$O)$_2$](H$_2$O)$_2$}$_n$ 1 (inia – isonicotinamide, C$_6$H$_6$N$_2$O), [Zn(inia)$_2$(HL)(H$_2$O)$_2$](H$_2$O) 2, Co(inia)(HL)(H$_2$O)$_5$ 3, {(CH$_6$N$_3$)$_2$[Cu(L)(H$_2$O)]$_2$(2OHpy)$_4$} 4 (2OHpy − 2-hydroxypyridine, C$_5$H$_5$NO; CH$_6$N$_3^+$ − guanidinium cation), and (CH$_6$N$_3$)Cu(L)(H$_2$O) 5. A single crystal XRD analysis reveals structural arrangement of 1, 2 and 4. CHN and IR analyses corroborate with the structural data and propose rational formulae also for 3 and 5. A strong antiferromagnetic (AFM) coupling is found for 4 (J = −116 cm$^{−1}$/mol Cu(II)) being in agreement with a pair short monoatomic  Cu•••O•••Cu’ coordination bridges (Cu•••O 1.941/ Cu’•••O 1.998 Å) showing pseudo dimers within coordination polyanions. As no such short contacts are seen for 1, the magnetically isolated Cu(II) are present in a neutral coordination formulae, while diamagnetic Zn(II) is in 2. Additionally, a strong AFM coupling is present also in 5 (J = −126 cm$^{−1}$/mol Cu(II)) with a formulae also suggesting ionic constituents as in 4. The cobalt compound 3 reveals only a small orbital contribution L within almost magnetically isolated Co(II), giving D = 56.5 cm$^{−1}$, E = −0.34 cm$^{−1}$, and zJ = −0.011 cm$^{−1}$.</dc:description><dc:date>2025</dc:date><dc:date>2025-03-10 14:38:15</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>167755</dc:identifier><dc:identifier>UDK: 546.56:546.73:547.541</dc:identifier><dc:identifier>ISSN pri članku: 0277-5387</dc:identifier><dc:identifier>DOI: 10.1016/j.poly.2025.117482</dc:identifier><dc:identifier>COBISS_ID: 228453891</dc:identifier><dc:language>sl</dc:language></metadata>
