Synthesis and Reactivity in Inorganic and Metal-organic Chemistry最新文献

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Synthesis, Spectroscopic Characterization: (IR, Multinuclear NMR, 119mSn Mössbauer and Mass Spectrometry), and Biological Activity (Antibacterial, Antifungal, and Cytotoxicity) of Di‐ and Triorganotin(IV) Complexes of (E)‐3‐(4‐Chlorophenyl)‐2‐phenylpropenoic Acid 合成,光谱表征:(IR,多核磁共振,119mSn Mössbauer和质谱),以及(E)‐3‐(4‐氯苯基)‐2‐苯基丙烯酸二和三有机锡(IV)配合物的生物活性(抗菌,抗真菌和细胞毒性)
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-09-01 DOI: 10.1081/SIM-200026257
Sadiq-ur-Rehman, Saqib Ali, A. Badshah, M. Mazhar, Xueqing Song, G. Eng, K. Khan
{"title":"Synthesis, Spectroscopic Characterization: (IR, Multinuclear NMR, 119mSn Mössbauer and Mass Spectrometry), and Biological Activity (Antibacterial, Antifungal, and Cytotoxicity) of Di‐ and Triorganotin(IV) Complexes of (E)‐3‐(4‐Chlorophenyl)‐2‐phenylpropenoic Acid","authors":"Sadiq-ur-Rehman, Saqib Ali, A. Badshah, M. Mazhar, Xueqing Song, G. Eng, K. Khan","doi":"10.1081/SIM-200026257","DOIUrl":"https://doi.org/10.1081/SIM-200026257","url":null,"abstract":"Abstract In an effort to develop new organotin(IV) compounds of industrial and biological importance, a series of di‐ and triorganotin(IV) complexes of (E)‐3‐(4‐chlorophenyl)‐2‐phenylpropenoic acid with the general formula R4‐n SnL n have been synthesized by the reaction of the corresponding organotin chlorides with the sodium salt of (E)‐3‐(4‐chlorophenyl)‐2‐phenylpropenoic acid (C15H10ClO2Na) where, R = CH3, C2H5, n‐C4H9, C6H5, C6H5 · CH2, n = 1 or 2 and L = acid anion (C15H10ClO2 −). The dimeric tetraorganodicarboxylatodistannoxanes [(Me2SnL)2O]2 compound (2) and [(Bu2SnL)2O]2 compound (4), L = C15H10ClO2 −, were synthesized by the reaction of R2SnO with the ligand acid (HL) in 1:1 molar ratio with azeotropic removal of water. The structures of the complexes are discussed on the basis of IR, multinuclear (1H, 13C, 119Sn) NMR, 119mSn Mössbauer spectroscopies and mass spectrometry. The spectroscopic results substantiate that all the diorganotin(IV) derivatives possess trigonal‐bipyramidal structures in solution and octahedral geometry in the solid state. A linear polymeric trigonal‐bipyramidal structure in the solid state and a tetrahedral environment around the tin atom in non‐coordinating solvents has been proposed for the triorganotin(IV) derivatives. The Δν [Δν = νasym(COO) − νsym(COO)] values obtained from the IR data, in comparison to the ligand acid and its sodium salt, fall in the range which shows that the ligand may act as a bidentate coordinating group through the carboxyl (COO) oxygen atoms. The biological activity and LD50 data of the synthesized compounds are also reported. The triorganotin(IV) complexes exhibit significantly better activities than the diorganotin(IV) derivatives. The LD50 data show that most of the investigated compounds are cytotoxic.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"2 1","pages":"1379 - 1399"},"PeriodicalIF":0.0,"publicationDate":"2004-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89697640","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Synthesis and Physicochemical Properties of Some β‐Ketoaminato Cobalt(II) Chelates and Their Adducts with 2,2′‐Bipyridine and 1,10‐Phenanthroline β -酮氨基钴(II)螯合物及其2,2′‐联吡啶和1,10‐菲罗啉加合物的合成和理化性质
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-09-01 DOI: 10.1081/SIM-200026294
J. Woods, A. Osowole, O. A. Odunola
{"title":"Synthesis and Physicochemical Properties of Some β‐Ketoaminato Cobalt(II) Chelates and Their Adducts with 2,2′‐Bipyridine and 1,10‐Phenanthroline","authors":"J. Woods, A. Osowole, O. A. Odunola","doi":"10.1081/SIM-200026294","DOIUrl":"https://doi.org/10.1081/SIM-200026294","url":null,"abstract":"Abstract The cobalt(II) β‐ketoamines complexes {Co[CH3C(O)CHC(CH3)NR]2; R = CH3, CH2(OH)CH2, C4H9} and ketoiminates {Co[CH3C(O)CH(CH3)C(‐N(CH2) n N‐)C(CH3)CHC(O)CH3]} and their adducts with 2,2′‐bipyridine (bipy) and 1,10‐phenanthroline (phen) have been synthesized and characterized by elemental analyses, magnetic susceptibility, conductivity, infrared, and electronic spectral measurements. The ligands coordinate to the cobalt ion in a bidentate manner using the N2O2 chromophore. The effective magnetic moments (μeff) observed for the complexes are in the range of 4.20–5.30 BM. Electronic spectra results and magnetic susceptibility measurements are consistent with the adoption of a four‐coordinate geometry for the cobalt(II) chelates and a six‐coordinate octahedral geometry for the 2,2′‐bipyridine and 1,10‐phenanthroline adducts. The available conductance data in nitromethane indicates that the compounds are non‐electrolytes.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"12 1","pages":"1471 - 1485"},"PeriodicalIF":0.0,"publicationDate":"2004-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76403763","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Azo Complexes of Cu(II), Co(II), Ni(II), Cd(II), Th(IV), and UO2(VI) Ions. Mixed‐Ligand Complexes, Pyrolysis Products and Biological Activity Cu(II)、Co(II)、Ni(II)、Cd(II)、Th(IV)和UO2(VI)离子的偶氮配合物。混合配体配合物、热解产物和生物活性
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-09-01 DOI: 10.1081/SIM-200026204
M. Mashaly, Atef T. Ramadan, B. A. El‐Shetary, Areej K. Dawoud
{"title":"Azo Complexes of Cu(II), Co(II), Ni(II), Cd(II), Th(IV), and UO2(VI) Ions. Mixed‐Ligand Complexes, Pyrolysis Products and Biological Activity","authors":"M. Mashaly, Atef T. Ramadan, B. A. El‐Shetary, Areej K. Dawoud","doi":"10.1081/SIM-200026204","DOIUrl":"https://doi.org/10.1081/SIM-200026204","url":null,"abstract":"Abstract The reactions of azo ligand, 2‐[2′‐carboxyphenylazo]‐5,5‐dimethyl‐1,3‐cyclohexane‐dione, (H2L), with the metal ion Cd(II), Cu(II), Ni(II), Co(II), Th(IV), or UO2(VI) in the presence of LiOH as a deprotonating agent, yielded binary mononuclear complexes. The binary Cu(II) complex reacts with the ligands 1,10‐phenanthroline or 2‐aminopyridine to form mixed‐ligand complexes. All the binary complexes of Cd(II), Cu(II), and Ni(II) have octahedral configurations, while the Co(II) complex is square‐planar. The binary complexes of Th(IV) and UO2(VI) have distorted dodecahedral geometries. The mixed‐ligand complexes have octahedral configurations. Thermal studies on these complexes showed the possibility of obtaining new complexes pyrolytically, where the complexes decompose through several isolable as well as non‐isolable intermediates during heating. The structures of all complexes and the corresponding thermal products were elucidated by elemental analyses, conductance, IR and electronic absorption spectra, magnetic moments, 1H NMR and TG–DSC measurements as well as by mass spectroscopy. The ligand and some of the complexes were found to activate the enzyme pectinlyase.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"12 1","pages":"1349 - 1378"},"PeriodicalIF":0.0,"publicationDate":"2004-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75233236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Studies on Some Thorium(IV) Complexes with High Coordination Numbers Derived from Semicarbazones of 4‐Aminoantipyrine 4 -氨基安替比林缩氨基脲类高配位数钍配合物的研究
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-09-01 DOI: 10.1081/SIM-200026274
R. Agarwal, I. Chakraborti, H. Agarwal
{"title":"Studies on Some Thorium(IV) Complexes with High Coordination Numbers Derived from Semicarbazones of 4‐Aminoantipyrine","authors":"R. Agarwal, I. Chakraborti, H. Agarwal","doi":"10.1081/SIM-200026274","DOIUrl":"https://doi.org/10.1081/SIM-200026274","url":null,"abstract":"Abstract The interaction of thorium(IV) salts with 4[N‐(benzylidene)amino]antipyrine semicarbazone (BAAPS), 4[N‐(4′‐methoxybenzylidene)amino]antipyrine semicarbazone (MBAAPS), 4[N‐(4′‐dimethoxyaminobenzylidene)amino]antipyrine semicarbazone (DABAAPS), 4[N‐(2′‐nitrobenzylidene)amino]antipyrine semicarbazone (2′‐NO2BAAPS), and 4[N‐(3′‐nitrobenzylidene)amino]antipyrine semicarbazone (3′‐NO2BAAPS) in non‐aqueous solvents resulted in the formation of [ThL2X4] (X = Cl, Br, or NCS), [ThL2I2]I2, [ThL2](ClO4)2 or [ThL(NO3)4] (L = BAAPS, MBAAPS, DABAAPS, 2‐NO2BAAPS, or 3‐NO2BAAPS). All of these compounds were characterized by elemental analyses, electrical conductivity, IR, and thermal methods. X‐ray powder diffraction studies of a representative complex were also undertaken. Th(IV) displays the coordination numbers 6, 8, 10, and 11 in these compounds depending on the nature of the coordinated anion and the stoichiometry.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"77 1","pages":"1431 - 1452"},"PeriodicalIF":0.0,"publicationDate":"2004-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79238822","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Synthesis and Physico‐Chemical Studies on 18‐Membered Octaazamacrocyclic Complexes of Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) Ions Mn(II)、Co(II)、Ni(II)、Cu(II)和Zn(II)离子十八元八杂环配合物的合成和物理化学研究
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-09-01 DOI: 10.1081/SIM-200026200
T. Khan, S. Tabassum, Y. Azim, M. Shakir
{"title":"Synthesis and Physico‐Chemical Studies on 18‐Membered Octaazamacrocyclic Complexes of Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) Ions","authors":"T. Khan, S. Tabassum, Y. Azim, M. Shakir","doi":"10.1081/SIM-200026200","DOIUrl":"https://doi.org/10.1081/SIM-200026200","url":null,"abstract":"Abstract A new series of 18‐membered octaazamacrocyclic complexes [ML1X2] and [ML2X2] (M = Mn(II), Co(II), Ni(II), Cu(II), and Zn(II); X = Cl or NO3) have been synthesized by template condensation of o‐phthalaldehyde with hydrazine hydrate and formaldehyde or acetaldehyde in MeOH. The nature of bonding and the stereochemistry of the complexes have been deduced from elemental analyses, FT‐IR, 1H NMR, EPR, UV spectroscopy, magnetic susceptibility, and conductivity measurements. An octahedral geometry has been suggested for all the complexes and the observed low molar conductance values indicate their non‐ionic nature.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"27 1","pages":"1305 - 1318"},"PeriodicalIF":0.0,"publicationDate":"2004-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88898323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Synthetic and Spectroscopic Studies of Some Nitrato–Lanthanide(III) Hydrazone Complexes of Higher Coordination Number 一些高配位数硝酸镧腙配合物的合成及光谱研究
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-09-01 DOI: 10.1081/SIM-200026268
D. Paschalidis
{"title":"Synthetic and Spectroscopic Studies of Some Nitrato–Lanthanide(III) Hydrazone Complexes of Higher Coordination Number","authors":"D. Paschalidis","doi":"10.1081/SIM-200026268","DOIUrl":"https://doi.org/10.1081/SIM-200026268","url":null,"abstract":"Abstract The reactions of the lanthanide(III) ions Y, La, Ce, Pr, Nd, Eu, Gd, Tb, Dy, Ho, Er, and Yb, with pyridine‐2‐carboxaldehyde‐4‐chlorobenzoylhydrazone (PpClBH) leads to the formation of complexes corresponding to the formulae [Ln(PpClBH)2(NO3)3], (Ln = La, Ce, and Pr) and [Ln(PpClBH)2(NO3)2]NO3 (Ln = Y, Nd, Eu, Gd, Tb, Dy, Ho, Er, and Yb). Twelve new compounds have been prepared. The complexes were characterized by means of elemental analyses, conductivity measurements, magnetic moments, and spectroscopic studies (IR, UV‐VIS, and 1H NMR). The coordination number of 12 have been proposed for the La, Ce, and Pr complexes, while for the Y, Nd, Eu, Gd, Tb, Dy, Ho, Er, and Yb compounds the coordination number is reduced to 10. This change in coordination number is consistent with the lanthanide contraction. Complexes having coordination numbers greater than ten appear to be limited to the lighter lanthanides. PpClBH has been characterized by elemental analysis, IR, UV, and 1H NMR.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"16 1","pages":"1401 - 1415"},"PeriodicalIF":0.0,"publicationDate":"2004-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80794611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Synthesis of a Novel Oxime Ligand: Characterization and Investigation of Its Complexes with Some Metal Ions 一种新型肟配体的合成及其与金属离子配合物的表征与研究
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-08-01 DOI: 10.1081/SIM-120039267
E. Taş, M. Ulusoy, M. Guler
{"title":"Synthesis of a Novel Oxime Ligand: Characterization and Investigation of Its Complexes with Some Metal Ions","authors":"E. Taş, M. Ulusoy, M. Guler","doi":"10.1081/SIM-120039267","DOIUrl":"https://doi.org/10.1081/SIM-120039267","url":null,"abstract":"Abstract A novel dioxime, 1,2‐dihydroxyimino‐3‐aza‐6‐morpholine heptane (H2L) was synthesized by the reaction of anti‐monochloroglyoxime and 4‐(3‐aminopropyl)morpholine in absolute THF. Mononuclear complexes with a metal:ligand ratio of 1:2 were prepared with Co(II), Cu(II), and Ni(II). The ligand and complexes were characterized by elemental analyses, FT‐IR, UV‐Vis, 1H NMR and 13C NMR spectra, magnetic susceptibility measurements. The thermal behavior of the compounds has been studied by thermogravimetry (TGA).","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"10 1","pages":"1211 - 1221"},"PeriodicalIF":0.0,"publicationDate":"2004-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84521810","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Synthesis and Magnetic Studies of μ‐Oxamido‐bridged Copper(II)–Manganese(II) Heterobinuclear Complexes μ -氧胺桥接铜(II) -锰(II)杂双核配合物的合成与磁性研究
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-08-01 DOI: 10.1081/SIM-120039264
Yan-Tuan Li, Cui‐Wei Yan, Chunyuan Zhu, H. Guan
{"title":"Synthesis and Magnetic Studies of μ‐Oxamido‐bridged Copper(II)–Manganese(II) Heterobinuclear Complexes","authors":"Yan-Tuan Li, Cui‐Wei Yan, Chunyuan Zhu, H. Guan","doi":"10.1081/SIM-120039264","DOIUrl":"https://doi.org/10.1081/SIM-120039264","url":null,"abstract":"Abstract Three new copper(II)–manganese(II) heterobinuclear complexes bridged by N,N′‐bis[2‐(dimethylamino)ethyl]oxamido dianion (dmoxae) and end‐capped with 5‐nitro‐1,10‐phenanthroline (NO2phen), 2,9‐dimethyl‐1,10‐phenanthroline (Me2phen) or 5‐phenyl‐1,10‐phenanthroline (Phphen), respectively; namely, [Cu(dmoxae)Mn(NO2phen)2](ClO4)2 (1), [Cu(dmoxae)Mn(Me2phen)2](ClO4)2 (2), and [Cu(dmoxae)Mn(Phphen)2](ClO4)2 (3); have been synthesized and characterized by elemental analyses, IR and electronic spectral studies and molar conductivity measurements. It is proposed that these complexes have oxamido‐bridged structures consisting of planar copper(II) and octahedral manganese(II) ions. The electronic reflectance spectra indicate the presence of exchange–coupling interaction between bridging copper(II) and manganese(II) ions. The cryomagnetic measurements (4.2–300 K) of the three complexes demonstrated the operation of antiferromagnetic interaction between the adjacent manganese(II) and copper(II) ions through the oxamido‐bridge within these copper(II)–manganese(II) heterobinuclear complexes. On the basis of the spin Hamiltonian, Hˆ= − 2Sˆ1 · Sˆ2, a magnetic analysis was carried out for the three complexes and the spin‐coupling constant (J) was evaluated as −39.7 cm−1 for (1), −38.5 cm−1 for (2), and −37.8 cm−1 for (3). The influence of methyl substituents in amine groups of the bridging ligand on magnetic interactions between the metal ions of this kind of complexes is also discussed.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"29 1","pages":"1165 - 1179"},"PeriodicalIF":0.0,"publicationDate":"2004-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90985177","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 24
Oxygen Atom Transfer Reactions to Metal Carbonyls: Kinetics and Mechanism of CO Substitution Reactions of M2(CO)9L (M = Re, L = PPh3, PMePh2, PMe2Ph, C5H5N, or M = Mn, L = C5H5N) in the Presence of (CH3)3NO (CH3)3NO存在下M2(CO)9L (M = Re, L = PPh3, PMePh2, PMe2Ph, C5H5N或M = Mn, L = C5H5N) CO取代反应的动力学和机理
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-08-01 DOI: 10.1081/SIM-120039265
Lijun Peng, Yici. Gao
{"title":"Oxygen Atom Transfer Reactions to Metal Carbonyls: Kinetics and Mechanism of CO Substitution Reactions of M2(CO)9L (M = Re, L = PPh3, PMePh2, PMe2Ph, C5H5N, or M = Mn, L = C5H5N) in the Presence of (CH3)3NO","authors":"Lijun Peng, Yici. Gao","doi":"10.1081/SIM-120039265","DOIUrl":"https://doi.org/10.1081/SIM-120039265","url":null,"abstract":"Abstract Rates for the reactions of M2(CO)9L (M = Re, L = PPh3, PMePh2, PMe2Ph, C5H5N or M = Mn, L = C5H5N) with L in the presence of (CH3)3NO as O‐atom transfer reagent and CHCl3 as solvent are reported. The reaction rates suggest a pathway of association (k 2). The reaction rate order of Re2(CO)9L with the four ligands is as follows: PPh3 > PMePh2 > PMe2Ph > C5H5N.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"34 1","pages":"1181 - 1190"},"PeriodicalIF":0.0,"publicationDate":"2004-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88604700","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis and Structure of the Mn(II) Complexes with Tripyrazolylborate Ligands: Mn[HB(pz)3]2 and Mn[HB(3,5‐Me2‐pz)3]2 Mn(II)三吡唑硼酸盐配合物Mn[HB(pz)3]2和Mn[HB(3,5‐Me2‐pz)3]2的合成和结构
Synthesis and Reactivity in Inorganic and Metal-organic Chemistry Pub Date : 2004-08-01 DOI: 10.1081/SIM-120039263
Y. Xing, K. Aoki, F. Bai
{"title":"Synthesis and Structure of the Mn(II) Complexes with Tripyrazolylborate Ligands: Mn[HB(pz)3]2 and Mn[HB(3,5‐Me2‐pz)3]2","authors":"Y. Xing, K. Aoki, F. Bai","doi":"10.1081/SIM-120039263","DOIUrl":"https://doi.org/10.1081/SIM-120039263","url":null,"abstract":"Abstract Mn(II) complexes Mn[HB(pz)3]2 (1) (pz = pyrazole) and Mn[HB(3,5‐Me2‐pz)3]2 (2) have been obtained by the reaction of Mn(OOCCH3)2 with NaHB(pz)3 and NaHB(3,5‐Me2‐pz)3 in MeOH, respectively. The two complexes (1) and (2) were characterized by IR, elemental analyses, and x‐ray diffraction. Complex (1) crystallizes in the space group C2/c, a = 18.971(3) Å, b = 13.700(3) Å, c = 19.056(3) Å, β = 111.378(10), V = 4612.0(13) Å3, Z = 2. Complex (2) crystallizes in the space group R‐3, a = 10.9832(18) Å, b = 10.983(2) Å, c = 24.785(3) Å, γ = 120°, V = 2589.3(7) Å3, Z = 3. X‐ray structure analysis has shown that the complexes (1) and (2) all are monomeric neutral complexes, and possess similar coordination modes around the metal Mn centers. In addition, some related bonding distances, angles, and structural properties are discussed.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"150 1","pages":"1149 - 1163"},"PeriodicalIF":0.0,"publicationDate":"2004-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86498357","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
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