Abstract

Copper(II) binuclear complexes [Cu(II)(1-phenylamidino-O-n-propylurea)tn]2 (H2O)2(Cl2)2 (1), [Cu(II)(1-phenylamidino-O-n-butylurea)tn]2(H2O)2(Cl2)2(2), [Cu(II)(1-phenylamidino-O-i-butylurea)tn]2(H2O)2(Cl2)2(3), and [Cu(II)(1-phenyamidino-O-i-butylurea)en]2(H2O)2(Cl2)2 (4) have been reported. The binuclear complexes 3 and 4 crystallize in a monoclinic structure with unit cell dimensions a = 15.252(17) A, b = 14.682(10) A, c = 13.606(13) A, and beta = 111.2(1) degrees and a = 15.278(35) A, b = 14.665(21) A, c = 13.603(27) A, and beta = 111.1(1) degrees , respectively. The EPR spectra of all the solid complexes at room temperature consisted of fine-structure transitions (DeltaM(s) = 1) with zero-field splitting (ZFS) of 0.0500 cm(-1) and a half-field signal (DeltaM(s) = 2) at ca. 1600 G, suggesting the formation of binuclear complexes (S = 1). From the observed ZFS, we estimated the average Cu-Cu distance. From the temperature dependence of the EPR signal intensity, we evaluated the isotropic exchange interaction constant J. It appears that the exchange interaction between the two interacting spins of the binuclear complexes is ferromagnetic in nature. The formation of ferromagnetically coupled copper binuclear complexes was further confirmed from the high magnetic-moment values at room temperature. When the EPR spectra were recorded in the temperature range 300-400 K, it was observed that the triplet-state EPR signal completely and irreversibly disappeared at ca. 380 K with the appearance of a new signal attributable to the mononuclear complex (S = 1/2). Thermal studies of these complexes in this temperature range suggested the loss of two water molecules, which might be responsible for binding two mononuclear species. EPR, IR, and thermal studies indicate a long-range ferromagnetic exchange mediated through hydrogen bonding between copper(II) ions (S = 1/2).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.