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1.
Inorg Chem ; 2020 Jun 08.
Artigo em Inglês | MEDLINE | ID: mdl-32510942

RESUMO

Reaction of the metalloligand IrIII(ppy-COOH)3 and the anisotropic paramagnetic CoII ion under solvothermal conditions resulted in a metal-metalloligand coordination polymer, [CoII3(µ3-O)(µ-OH2){IrIII(ppy-COO)2(ppy-COOH)}2(H2O)4]·2DMF·xH2O (I). It consists of trimeric Co3O secondary building units (SBUs) bridged by pairs of Ir to form chains of alternate orthogonal squares. The compound undergoes two single-crystal to single-crystal transformations while retaining its general structural features. A chemical transformation occurs to give [CoII3(µ3-O){IrIII(ppy-COO)2(ppy-COOH)}2(H2O)4(DMF)]·DMF·H2O (II) by soaking in acetone, where a bridging water molecule departs and the solvent DMF bonds to the vacant site of the Co center. Both I and II undergo a temperature-induced transformation to [CoII3(µ3-O){IrIII(ppy-COO)2(ppy-COOH)}2(H2O)3(DMF)]·DMF (III), where one more coordinated water molecule is lost. The major difference in the three phases is in the Co coordination spheres, which have considerable consequences on the magnetism. Compound I displays paramagnetism down to 2 K, whereas II and III show weak ferromagnetism with TC values of 14 and 17 K, respectively.

2.
Leuk Lymphoma ; : 1-8, 2020 Jun 14.
Artigo em Inglês | MEDLINE | ID: mdl-32536235

RESUMO

The prognosis of patients with acute myeloid leukemia (AML) caused by the FLT3-ITD mutation is poor. Arsenic trioxide (ATO) and all-trans retinoic acid (ATRA) can down-regulate FLT3-ITD level and selectively kill leukemia cells carrying the FLT3-ITD mutation. However, the mechanisms of action of these two compounds are unknown. Here, we found that ATO could bind FLT3-ITD at Lys91 and Asp225, whereas ATRA could bind FLT3-ITD at Lys5 and Gln6. Both compounds could not bind wild-type FLT3. Further studies revealed that ATO/ATRA may suppress the Expression of FLT3-ITD by promoting the UBE2L6-mediated ubiquitination pathway and decreasing the expression of C-MYC. However, further studies are needed to define the mechanisms of these compounds on AML. Our research provides an experimental basis for the use of ATO/ATRA in FLT3-ITD AML in clinical practice.

3.
Dalton Trans ; 2020 Mar 05.
Artigo em Inglês | MEDLINE | ID: mdl-32134093

RESUMO

Photochemical reactions of (PPh4)[OsVI(N)(L)(CN)3] (NO2-OsN) with piperidine and pyrrolidine afforded two osmium(v) hydrazido compounds, (PPh4)[OsV(L)(CN)3(NNC5H10)] ([PPh4]1) and (PPh4)[OsV(L)(CN)3(NNC4H8)] ([PPh4]2), respectively. Their structures consist of isolated, mononuclear distorted octahedral osmium anions that are well-separated from each other by PPh4+. Their low spin S = 1/2 and L = 1 ground state was confirmed by magnetometry and DFT calculations. Interestingly, both compounds exhibit slow magnetic relaxation under a bias dc-field. These osmium(v) complexes are potentially useful building-blocks for the construction of molecule-based architectures with interesting magnetic properties. In contrast, the structurally related (PPh4)[OsIII(L)(CN)3(NH3)] ([PPh4]3), which also has a low-spin S = 1/2 ground state but with a different electronic configuration (5d5), does not exhibit slow magnetic relaxation, due to the absence of any orbital moment (L = 0). Furthermore, the structurally different osmium(v) hydrazido compound reported by Meyer, [OsV(tpy)(Cl)2(NNC5H10)](PF6) (4[PF6]), also does not exhibit slow magnetic relaxation due possibly to a change in magnetic anisotropy from axial for [PPh4]1 and [PPh4]2 to planar.

4.
Dalton Trans ; 49(12): 3758-3765, 2020 Mar 28.
Artigo em Inglês | MEDLINE | ID: mdl-31761912

RESUMO

Reactions of metalloligands MIII(notpH3) (M = Fe, Co and notpH6 = 1,4,7-triazacyclononane-1,4,7-triyl-tris(methylenephosphonic acid)) with Zn(OAc)2 under hydrothermal conditions resulted in new metal phosphonates Zn2Fe(notp)Cl(H2O) (1) and ZnCo(notpH)(H2O)·2H2O (2). They crystallize in polar space groups P63 (for 1) and Pca21 (for 2), respectively, and exhibit layer structures in which the inorganic layers are separated by the organic groups of the notp ligands. However, the layer topologies of the two compounds are quite different. In 1, the layer contains 6-membered rings composed of one {FeN3O3} octahedron, one {Zn1O3Cl}, one {Zn2O4} and three {PO3C} tetrahedra via corner-sharing connections, while in 2, the layer contains 10-membered rings composed of two {CoO3N3} octahedra, three {ZnO4} and five {PO3C} tetrahedra via vertex-sharing connections. Dielectric measurements on single crystals of 2 confirmed the presence of high dielectric anisotropy. Proton conductivity measurements revealed that the proton conduction is more favourable in 2 due to the presence of a continuous hydrogen bond network in this compound.

5.
Chem Commun (Camb) ; 55(92): 13920-13923, 2019 Nov 14.
Artigo em Inglês | MEDLINE | ID: mdl-31682247

RESUMO

Bimetallic MOF precursors can produce a homogeneous distribution of mixed-metal oxides after calcination, and thus may provide high efficiency as electrocatalysts in the water splitting process. We designed a layered bimetallic-organophosphonate containing Ir, Co and P because the metal-oxides are well-known for their efficiency in the oxygen-evolution reaction (OER), especially when the phosphate acts as a proton carrier. We describe the structure of the MOF and characteristics of the calcined form, which has outstanding OER characteristics in 1.0 M KOH with an overpotential of 317.7 mV at 10 mA cm-2 and a low Tafel slope of 59.1 mV dec-1.

6.
Int J Mol Sci ; 20(20)2019 Oct 09.
Artigo em Inglês | MEDLINE | ID: mdl-31600869

RESUMO

Tomato chlorosis virus (ToCV) is widespread, seriously impacting tomato production throughout the world. ToCV is semi-persistently transmitted by Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae). Currently, insect olfaction is being studied to develop novel pest control technologies to effectively control B. tabaci and whitefly-borne virus diseases. Despite current research efforts, no report has been published on the role of odorant-binding proteins (OBPs) in insect preference under the influence of plant virus. Our previous research showed that viruliferous B. tabaci preferred healthy plants at 48 h after virus acquisition. In this study, we determined the effect of OBPs on the host preference interactions of ToCV and whiteflies. Our results show that with the increase in acquisition time, the OBP gene expressions changed differently, and the OBP3 gene expression showed a trend of first rising and then falling, and reached the maximum at 48 h. These results indicate that OBP3 may participate in the host preference of viruliferous whiteflies to healthy plants. When the expression of the OBP3 gene was knocked down by an RNA interference (RNAi) technique, viruliferous Mediterranean (MED) showed no preference and the ToCV transmission rate was reduced by 83.3%. We conclude that OBP3 is involved in the detection of plant volatiles by viruliferous MED. Our results provide a theoretical basis and technical support for clarifying the transmission mechanism of ToCV by B. tabaci and could provide new avenues for controlling this plant virus and its vectors.


Assuntos
Crinivirus/fisiologia , Inativação Gênica , Insetos Vetores/genética , Insetos Vetores/virologia , Interferência de RNA , Receptores Odorantes/genética , Animais , Transmissão de Doença Infecciosa , Genes Reporter , Hemípteros/virologia , Interações Hospedeiro-Patógeno/genética , Lycopersicon esculentum/virologia , Doenças das Plantas/virologia
7.
ACS Omega ; 4(15): 16543-16550, 2019 Oct 08.
Artigo em Inglês | MEDLINE | ID: mdl-31616834

RESUMO

The incorporation of phosphonate ligands into the cyclometalated iridium(III) complexes can not only tune their electronic and optical properties but also provide the possibility of anchoring these molecules on the semiconductor surfaces for further applications. Herein, we report the first examples of mononuclear cyclometallated iridium(III) complexes incorporating phosphonate ligands, namely, [Ir(ppy)2(HL1)]·0.5H2O (1), [Ir(ppy)2(HL2)]·0.5H2O (2), [Ir(dfppy)2(HL1)] (3), and [Ir(dfppy)2(HL2)]·3.5H2O (4) (ppy = 2-phenylpyridine, dfppy = 2-(2,4-difluorophenyl)pyridine, H2L1 = 2-pyridylphosphonic acid, H2L2 = 2-quinolinephosphonic acid). Luminescent spectra are studied both in solution and in the solid state, and significantly red-shifted broad emission bands are observed in complexes 2 and 4. The experimental and density functional theory (DFT) time-dependent-DFT calculation results indicate that the expansion of the aromatic conjugation length in the ancillary phosphonate ligands decreases the lowest unoccupied molecular orbital energy levels of the systems, originating from the triplet state associated with the ancillary ligand such as 3MLCT, 3LC, and 3LLCT charge-transfer transitions.

8.
Inorg Chem ; 58(20): 14034-14045, 2019 Oct 21.
Artigo em Inglês | MEDLINE | ID: mdl-31560533

RESUMO

By virtue of its magnetic moment and variable valencies, the D4h paddlewheel ruthenium dimer is a desirable molecular building block for the construction of functional networks. If in addition to the Ru open axial site the organic ligand is designed to allow transversal connections, a wider range of structural possibilities is expected. The organic ligand can also be modified to introduce other functionalities. In the present study we employed a diphosphonate containing a protonated amine, 1-ammoniummethylenediphosphonate [NH3CH(PO3)23-; (Hamdp)], as the ligand to construct paddlewheel Ru2(Hamdp)2 building block. Three networks of different structural dimensionalities were obtained. (H3O)2[RuII2(Hamdp)2] (1) forms one-dimensional chain of S = 1 RuII2 bridged at axial positions through Ru-O bonds. From 1 as a starting material, its reaction with lanthanide ions results in the bimetallic Dy(H2O)3[Ru2(Hamdp)2][Ru2(Hamdp)2(H2O)2][Ru2(Hamdp)(amdp)]0.5·12H2O (2), which has a pillared-bilayer structure and Yb[Ru2(Hamdp)2]2[Ru2(Hamdp)2(H2O)2]·15H2O (3), which is a three-dimensional open framework, both contain mixed-valent RuII/III2 units and show new connection topologies of the Ru2 dimers. After activation 2 does not adsorb N2 and CO2 but takes up 12 H2O. In contrast, 3 take up all three gases. The optimum proton conductivities were moderate reaching 1.44 × 10-6 for 2 and 0.93 × 10-5 S cm-1 for 3 at 95% relative humidity and 55 °C.

9.
Dalton Trans ; 48(36): 13769-13779, 2019 Sep 17.
Artigo em Inglês | MEDLINE | ID: mdl-31482159

RESUMO

Systematic control of the intermolecular pair-wise [4 + 4] photocycloaddition of a series of dysprosium phosphonates through fine-tuning of two different phosphonate ligands, one with a bidentate blocker and one with an anthracene antenna, both with alkyl substituents, reveals a size dependent rate. With bulky isopropyl on the diphosphonate blocker little response to UV light is observed. In contrast, compounds with ethyl which has less steric hindrance exhibit almost complete photocycloaddition. Interestingly, the alkyl substituents attached to anthracene monophosphonate have no evident effect on the reaction rate. Although no direct relationship can be found between the substitutions and the observed differences in field-induced single molecule magnetism, remarkable changes in magnetic dynamics are observed for complexes before and after the complete photocycloaddition reactions.

10.
Dalton Trans ; 48(19): 6539-6545, 2019 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-31011721

RESUMO

Three polymorphic copper carboxylate-phosphonates are reported, namely, α-Cu(4-cnappH)(H2O) (α-Cu-1), α-Cu(4-cnappH)(H2O)·0.5H2O (α-Cu-2) and ß-Cu(4-cnappH)(H2O) (ß-Cu), where 4-cnappH3 is (4-carboxynaphthalen-1-yl)phosphonic acid. All show layer structures but with different layer topologies. The layer topologies of the α-phases are similar, where the distorted {CuO4} planes and {PO3C} tetrahedra are corner-shared forming an inorganic layer containing 8- and 16-member rings. In ß-Cu, double chains made up of corner-sharing {CuO5} and {PO3C} are crossed-linked through edge-sharing of the {CuO5} square pyramids to form an inorganic layer containing 4- and 8-member rings. The uncoordinated carboxylate groups are protonated and are involved in the interlayer hydrogen bonds in all cases. Antiferromagnetic interactions are dominant in all cases. Compounds α-Cu-1, α-Cu-2 and ß-Cu can be exfoliated in THF resulting in 2D nanosheets of mainly two-layer thickness. Proton conductivity measurements reveal that the proton conduction is more favorable in α-Cu-2 than in α-Cu-1, but exfoliation into nanosheets decreases the conductivity.

11.
ACS Appl Mater Interfaces ; 11(13): 12986-12992, 2019 Apr 03.
Artigo em Inglês | MEDLINE | ID: mdl-30860352

RESUMO

Two-dimensional (2D) nanomaterials are remarkably attractive platform candidates for signal transduction through fluorescence resonance energy transfer or photo-induced electron-transfer pathway. In this work, a 2D Hofmann metal organic framework (hMOF) monolayer nanosheet was developed as an axial coordination platform for DNA detection via a ligand-to-metal charge-transfer quenching mechanism. Through modulating the position of phosphonate groups of rigid ligands, a layer-structured hMOF was synthesized. The single crystals showed that the adjacent layers were linked via hydrogen bonds between diethyl 4-pyridylphosphonate and the solvent. Furthermore, the 2D hMOF monolayer nanosheets were obtained easily via a top-down method. More significantly, the quenching mechanism was identified as an axial coordination between the open Fe2+ sites of hMOF nanosheets and fluorophores with 91% quenching efficiency, constituting an excellent signal transduction strategy. The smart use of hMOF monolayer nanosheets as an axial coordination platform could lead to promising applications in signal switching or/and sensing devices.


Assuntos
DNA/análise , Transferência Ressonante de Energia de Fluorescência/métodos , Corantes Fluorescentes/química , Estruturas Metalorgânicas/química , Nanoestruturas/química , DNA/química
12.
Chem Commun (Camb) ; 55(19): 2825-2828, 2019 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-30766989

RESUMO

Homochiral iron(ii)-based nanotubular metal phosphonates (R)- and (S)-[Fe(pemp)(H2O)2] [pemp2- = (R)- or (S)-(1-phenylethylamino)methylphosphonate] are reported showing metamagnetism at low temperature. The dehydrated product features coordinatively unsaturated and redox-active metal ion sites that enable it to strongly bind nitric oxide at room temperature.

13.
Dalton Trans ; 48(8): 2735-2740, 2019 Feb 19.
Artigo em Inglês | MEDLINE | ID: mdl-30724312

RESUMO

Four mononuclear lanthanide complexes, [Ln(depma)2(H2O)6]Cl3·xH2O·yCH3OH [Ln = Dy (1Dy), x = 6, y = 0; Gd (2Gd), x = 3, y = 1; Er (3Er), x = 6, y = 0; Yb (4Yb), x = 3, y = 1; depma = 9-diethylphosphono-methylanthracene], are reported and structurally characterized. The octa-coordinated environment of LnIII is composed of two oxygen atoms from two different depma ligands and six oxygen atoms from each bound water molecule. All four complexes show photoluminescence in the solid state at room temperature, originating from the ligand-centered emissions of depma. Furthermore, slow magnetization relaxation is found in 1Dy, 3Er and 4Yb with the energy barriers (Ueff) of 40.5 K (1 kOe), 9.8 K (1 kOe) and 28.9 K (0.75 kOe), respectively.

14.
Chem Sci ; 9(30): 6424-6433, 2018 Aug 14.
Artigo em Inglês | MEDLINE | ID: mdl-30310572

RESUMO

{Dy5(EDDC)2(µ3-AcO)2(µ5-C15H11PO3)(µ4-C15H11PO3)(µ2-AcO)2(AcO)2(H2O)(CH3OH)2}2(µ4-C2O4)·xH2O (I), where H2EDDC is N',N'',E,N',N'',E-N',N''-(ethane-1,2-diylidene)dipyrazine-2-carbohydrazide and C15H11PO3H2 is 9-anthrylmethylphosphonic acid, is found to undergo two consecutive single-crystal-to-single-crystal transformations. The first is under UV irradiation (λ = 365 nm for 3 d in air) to {Dy5(EDDC)2(µ3-AcO)2(µ5-C15H11PO3)2(µ2-AcO)2(AcO)2(H2O)3}2(µ4-C2O4)·xH2O (I-UV) where the two CH3OH are replaced by two H2O and the second by annealing under N2 at 100 °C on a diffractometer or under Ar in a glovebox to {Dy5(EDDC)2(µ3-AcO)2(µ5-C15H11PO3)2(µ2-AcO)4(H2O)}2(µ4-C2O4) (I-A-N2 or I-A-Ar) where it has lost two H2O molecules. The second transformation is reversible by exposure to air at room temperature (I-A-N2-cool). While the overall structures are the same (retaining the space group P21/c), there is a considerable expansion of the unit cell from I (8171 Å3) to I-UV (8609 Å3) and I-A-N2 (8610 Å3) and the coordinations of the Dy atoms undergo major reconstructions. This is associated with switching the single-molecule-magnetism (SMM) from OFF for I to ON for I-UV and to OFF again for I-A-Ar in air. Such a switching mechanism associated with the retention of crystallinity is unique in the chemistry of dysprosium. The structure of the molecule is formed from two symmetry related pentamers joined by an oxalate. A related compound containing two isolated neutral pentamers {Dy5(EDDC)2(µ3-AcO)2(µ5-C15H11PO3)2(µ2-AcO)3(AcO)2(H2O)2}{Dy5(EDDC)2(µ3-AcO)2(µ5-C15H11PO3)(µ4-C15H11PO3)(µ2-AcO)3(AcO)2(CH3OH)2}·2CHCl3 (II) has also been isolated with closely related Dy coordination and it exhibits similar SMM behaviour in zero field.

15.
Inorg Chem ; 57(21): 13252-13258, 2018 Nov 05.
Artigo em Inglês | MEDLINE | ID: mdl-30338990

RESUMO

Iridium(IV) oxides have gained increased attention in recent years owing to the presence of competing spin-orbit coupling and Coulomb interactions, which facilitate the emergence of novel quantum phenomena. In contrast, the electronic structure and magnetic properties of IrIV-based molecular materials remain largely unexplored. In this paper, we take a fresh look at an old but puzzling compound, Na2IrCl6, which can be hydrated to form two stable phases with formulas Na2IrCl6·2H2O and Na2IrCl6·6H2O. Their crystal structures are well illustrated based on X-ray powder diffraction data. Magnetic studies reveal that Na2IrCl6 and Na2IrCl6·2H2O are canted antiferromagnets with ordering temperatures of 7.4 and 2.7 K, respectively, whereas Na2IrCl6·6H2O is paramagnetic down to 1.8 K. First-principle calculations on Na2IrCl6 reveal a Jeff = 1/2 ground state, and the band structures show that Na2IrCl6 is a spin-orbital-induced semiconductor with an indirect gap of about 0.18 eV.

16.
Inorg Chem ; 57(19): 12143-12154, 2018 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-30226764

RESUMO

Four pairs of enantiomeric dysprosium(III) phosphonates, namely, R- or S-[Dy3(pempH2)2(pempH)7]2(NO3)4·12H2O ( R-1 or S-1), R- or S-[Dy3(pempH)7(pempH2)2]Cl2·2H2O ( R-2 or S-2), R- or S-[Dy3(pempH)7(pempH2)2]Br2·2H2O ( R-3 or S-3), and R- or S-[Dy11(pempH2)6(pempH)27](CF3SO3)6·22H2O ( R-4 or S-4) are reported, where R- or S-pempH2 represent R- or S-(1-phenylethyl)amino] methylphosphonic acid. All show homochiral chain structures, charge-balanced by counteranions. A comparison of the crystal morphologies of the R-isomers reveals that the overall shapes are quite similar for the four compounds, but the aspect ratio changes remarkably following the sequence: R-1 < R-2 < R-3 < R-4. The sequence is in agreement with the decreasing interchain interactions related to different counteranions, which is rationalized by molecular simulations. The counteranions also influence the intrachain structures and the local coordination environments of the DyIII ions. As a result, compounds R-2 and R-3 exhibit distinct dual relaxation processes at zero dc field with the effective energy barriers for the slow- and fast-relaxation being 79.1 and 37.6 K for R-2, and 80.0 and 39.1 K for R-3, respectively. For compounds R-1 and R-4, however, slow magnetic relaxation is also observed at zero dc field but without the appearance of maxima down to 1.8 K.

17.
Oncol Lett ; 16(2): 1439-1448, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-30008822

RESUMO

Gliomas are the most common type of malignant primary brain tumors in adults and exhibit a spectrum of aberrantly aggressive phenotypes. Despite advances in treatments during past decades, prognosis of the disease remains poor, with a median survival time of 12-14 months. Future studies on the molecular mechanism of the disease may provide the theoretical basis to identify new targets for effective therapies. The present study revealed that in glioblastoma cells, the overexpression of cytochrome P450, family 27, subfamily A, polypeptide 1 (CYP27A1) promoted proliferation, while silencing of CYP27A1 inhibited proliferation, without affecting migration and invasion. CYP27A1 protein was upregulated in glioblastoma tissues, indicating that CYP27A1 is an oncogene. The downregulation of specific microRNAs (miRNA) may contribute to the upregulation of oncogenes in glioblastoma. A common strategy was used to predict target miRNAs of CPY27A1 using the miRanda algorithm. miR-211 and miR-204 could target the 3'untranslated region of CPY27A1 mRNA. Additional studies confirmed that the overexpression of miR-204 inhibited CPY27A1 expression in glioblastoma cells. Finally, it was identified that miR-204 was downregulated in glioblastoma and that its overexpression inhibited proliferation, migration and invasion in glioblastoma cells. Thus, it was concluded that miR-204 functions as a tumor suppressor gene, at least partly by suppressing CYP27A1 in glioblastoma.

18.
Chem Commun (Camb) ; 54(49): 6276-6279, 2018 Jun 14.
Artigo em Inglês | MEDLINE | ID: mdl-29850696

RESUMO

The reaction of copper(ii) chloride with 2-carboxyphenylphosphonic acid (2-cppH3) under hydrothermal conditions at 100 °C results in the formation of a polar compound, Cu3(2-cpp)2(H2O)5 (1), which shows large dielectric anisotropy. A similar reaction at 140 °C results in a centrosymmetric phase, Cu3(2-cpp)2(H2O)2 (2). Compound 1 can convert into 2 upon increasing the reaction temperature under hydrothermal conditions, and further to Cu3(2-cpp)2 (3) upon thermal treatment at 240 °C. This process is accompanied by a switch from ferromagnetic in 1 to antiferromagnetic interactions in 2 and 3.

19.
Chemistry ; 24(51): 13495-13503, 2018 Sep 12.
Artigo em Inglês | MEDLINE | ID: mdl-29947086

RESUMO

By introducing the polar methoxy group into phenyl- or benzyl-phosphonate ligands, four cobalt phosphonates with layered structures are obtained, namely, [Co(4-mopp)(H2 O)] (1), [Co(4-mobp)(H2 O)] (2), [Co(3-mopp)(H2 O)] (3), and [Co(3-mobp)(H2 O)] (4), where 4- or 3-moppH2 is (4- or 3-methoxyphenyl)phosphonic acid and 4- or 3-mobpH2 is (4- or 3-methoxybenzyl)phosphonic acid. Compounds 1, 2, and 4 crystallize in the polar space groups Pmn21 or Pna21 , whereas compound 3 crystallizes in the centrosymmetric space group P21 /n. The layer topologies in the four structures are similar and can be viewed as perovskite type, where the edge-sharing [Co4 O4 ] rhombi are capped by the PO3 C groups. The phenyl and MeO groups in compounds 1-3 are heavily disordered, whereas that in 4 is ordered. Structural comparison based on the data at 296 and 123 K reveals distinct dynamic motion of the organic groups in compounds 1 and 2. The fluctuation of the polar MeO groups in these two compounds is confirmed by dielectric relaxation measurements. In contrast, the fluctuation of polar groups in compounds 3 and 4 is not evident. Interestingly, the dehydrated samples of 3 and 4 (i.e., 3-de and 4-de) exhibit one-step and two-step phase transitions associated with the motion of polar organic groups, as proven by DSC and dielectric measurements. The magnetic properties of compounds 1-4 are investigated, and strong antiferromagnetic interactions are found to mediate between the magnetic centers through µ-O(P) and O-P-O bridges.

20.
Angew Chem Int Ed Engl ; 57(28): 8577-8581, 2018 07 09.
Artigo em Inglês | MEDLINE | ID: mdl-29757484

RESUMO

In search of magneto-optic materials, the mononuclear compounds LnIII (depma)(NO3 )3 (hmpa)2 (Ln=Dy, Gd) were synthesized. The anthracene moieties undergo [4+4] dimerization when irradiated at 365 nm without loss of crystallinity. The Dy compound switches from a single-ion to a single-molecule magnet with doubling of the spin reversal barrier energy and from yellow-green to blue-white emission. The dimerization is reversed by heating at 100 °C or partially on light irradiating at 254 nm. The results suggest that lanthanide phosphonates with anthracene are promising smart materials displaying synergistic magneto-optic property.

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