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  1. Free, publicly-accessible full text available May 3, 2024
  2. Herein we report heteroleptic Co( ii ) diimine complexes [Co(H 2 bip) 2 Cl 2 ] ( 1 ), [Co(H 2 bip) 2 Br 2 ] ( 2 ), [Co(H 2 bip) 3 ]Br 2 ·1MeOH ( 3 ) and [Co(H 2 bip) 2 (Me 2 bpy)]Br 2 ·(MeCN) 0.5 ·(H 2 O) 0.25 ( 4 ) (H 2 bip = 2,2′-bi-1,4,5,6-tetrahydropyrimidine, bpy = 2,2′-dipyridyl, Me 2 bpy = 4,4′-Me-2,2′-dipyridyl), purposefully prepared to enable a systematic study of magnetic property changes arising from the increase of overall ligand field from σ/π-donor chlorido ( 1 ) to π-acceptor 4,4′Me-2,2′bpy ( 4 ). The presence of axial and rhombic anisotropy ( D and E ) of these compounds is sufficient to allow 1–4 to show field-induced slow relaxation of magnetization. Interestingly, we found as the effective ligand field is increased in the series, rhombicity ( E / D ) decreases, and the magnetic relaxation profile changes significantly, where relaxation of magnetization at a specific temperature becomes gradually faster. We performed mechanistic analyses of the temperature dependence of magnetic relaxation times considering Orbach relaxation processes, Raman-like relaxation and quantum tunnelling of magnetization (QTM). The effective energy barrier of the Orbach relaxation process ( U eff ) is largest in compound 1 (19.2 cm −1 ) and gradually decreases in the order 1 > 2 > 3 > 4 giving a minimum value in compound 4 (8.3 cm −1 ), where the Raman-like mechanism showed the possibility of different types of phonon activity below and above ∼2.5 K. As a precursor of 1 , the tetrahedral complex [Co(H 2 bip)Cl 2 ] ( 1a ) was also synthesized and structurally and magnetically characterized: this compound exhibits slow relaxation of magnetization under an applied dc field (1800 Oe) with a record slow relaxation time of 3.39 s at 1.8 K. 
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  3. null (Ed.)
    The new PtVO(SOCR) 4 lantern complexes, 1 (R = CH 3 ) and 2 (R = Ph) behave as neutral O-donor ligands to Ln(OR) 3 with Ln = Ce, Nd. Four heterotrimetallic complexes with linear {LnOVPt} units were prepared: [Ln(ODtbp) 3 {PtVO(SOCR) 4 }] (Ln = Ce, 3Ce (R = CH 3 ), 4Ce (R = Ph); Nd, 3Nd (R = CH 3 ), 4Nd (R = Ph); ODtbp = 2,6-ditertbutylphenolate). Magnetic characterization confirms slow magnetic relaxation behaviour and suggests antiferromagnetic coupling across {Ln–OV} in all four complexes, with variations tunable as a function of Ln and R. 
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