Fine-tuning the effects of auxiliary ligands on two trigonal-bipyramid cobalt(ii) complexes exhibiting field-induced slow magnetic relaxation. (23rd April 2018)
- Record Type:
- Journal Article
- Title:
- Fine-tuning the effects of auxiliary ligands on two trigonal-bipyramid cobalt(ii) complexes exhibiting field-induced slow magnetic relaxation. (23rd April 2018)
- Main Title:
- Fine-tuning the effects of auxiliary ligands on two trigonal-bipyramid cobalt(ii) complexes exhibiting field-induced slow magnetic relaxation
- Authors:
- Hou, Xiangyang
Wang, Xiao
Liu, Xiangyu
Wang, Jijiang
Tang, Long
Ju, Ping - Abstract:
- Abstract : Two trigonal-bipyramid cobalt(ii ) complexes exhibit field-induced slow magnetic relaxation effects due to their auxiliary ligands. Abstract : Two penta-coordinate Co 2+ complexes, namely [Co(PDA)(H2 O)2 ] (1 ) and [Co(PDA)(1, 2-BIYB)0.5 (H2 O)]·(H2 O) (2 ), (H2 PDA = pyridine-3, 5-dicarboxylate, 1, 2-BIYB = 1, 2-bis(imidazol-1-ylmethyl) benzene), which have similar ligand fields except for their local symmetries due to the different coordination atoms of Co 2+, were synthesized, structurally analyzed, and magnetically investigated. Complexes1 and2 possess 3D supramolecular structures in which the 2D structures are further cross-linked by hydrogen bonds. Complex1 can be observed to transform into2 in the presence of 1, 2-BIYB coligand, and1 and2 have distortion trigonal bipyramid geometries when the space group of Co 2+ ion changes from C 2/ c in1 to P 2(1)/ c in2 . Meanwhile, the average equatorial Co–O/N bond distances of CP1 (2.1655 Å) are clearly larger than its axial Co–O bond distances (2.0704 Å); for CP2, the average equatorial Co–O/N bond distances (2.0814 Å) are slightly shorter than the axial Co–O/N bond distances (2.0896 Å), which leads to different axial compression and distortion of the trigonal bipyramid metal environment. Fine-tuning of the structures arising from the auxiliary ligands has a definite impact on the magnetic properties of compounds1 and2 . Both compounds share easy-plane magnetic anisotropies of their central Co 2+ ions ( D = 16 cm −1Abstract : Two trigonal-bipyramid cobalt(ii ) complexes exhibit field-induced slow magnetic relaxation effects due to their auxiliary ligands. Abstract : Two penta-coordinate Co 2+ complexes, namely [Co(PDA)(H2 O)2 ] (1 ) and [Co(PDA)(1, 2-BIYB)0.5 (H2 O)]·(H2 O) (2 ), (H2 PDA = pyridine-3, 5-dicarboxylate, 1, 2-BIYB = 1, 2-bis(imidazol-1-ylmethyl) benzene), which have similar ligand fields except for their local symmetries due to the different coordination atoms of Co 2+, were synthesized, structurally analyzed, and magnetically investigated. Complexes1 and2 possess 3D supramolecular structures in which the 2D structures are further cross-linked by hydrogen bonds. Complex1 can be observed to transform into2 in the presence of 1, 2-BIYB coligand, and1 and2 have distortion trigonal bipyramid geometries when the space group of Co 2+ ion changes from C 2/ c in1 to P 2(1)/ c in2 . Meanwhile, the average equatorial Co–O/N bond distances of CP1 (2.1655 Å) are clearly larger than its axial Co–O bond distances (2.0704 Å); for CP2, the average equatorial Co–O/N bond distances (2.0814 Å) are slightly shorter than the axial Co–O/N bond distances (2.0896 Å), which leads to different axial compression and distortion of the trigonal bipyramid metal environment. Fine-tuning of the structures arising from the auxiliary ligands has a definite impact on the magnetic properties of compounds1 and2 . Both compounds share easy-plane magnetic anisotropies of their central Co 2+ ions ( D = 16 cm −1 for1 and D = 59 cm −1 for2 ) and different slow magnetic relaxations of magnetization with applied magnetic fields of 1500 Oe and 3000 Oe, respectively. … (more)
- Is Part Of:
- New journal of chemistry. Volume 42:Number 11(2018)
- Journal:
- New journal of chemistry
- Issue:
- Volume 42:Number 11(2018)
- Issue Display:
- Volume 42, Issue 11 (2018)
- Year:
- 2018
- Volume:
- 42
- Issue:
- 11
- Issue Sort Value:
- 2018-0042-0011-0000
- Page Start:
- 8583
- Page End:
- 8590
- Publication Date:
- 2018-04-23
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c8nj01201f ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6947.xml