Theoretical study of stability, structures, and aromaticity of multiply N-confused porphyrins.

The total electronic energy and nucleus-independent chemical shift (NICS) of 95 isomers of N-confused porphyrin (NCP: normal porphyrin (N(0)CP), singly N-confused porphyrin (N(1)CP), doubly N-confused porphyrin (N(2)CP), triply N-confused porphyrin (N(3)CP), and fully N-confused porphyrin (N(4)CP)) have been calculated by the density functional theory (DFT) method. The stability of NCP decreased by increasing the number of confused pyrrole rings. Namely, the relative energies of the most stable isomers in each confusion level increased in a stepwise manner approximately by +18 kcal/mol: 0 (N(0)CP1), +17.147 (N(1)CP2), +37.461 (N(2)CPb3), +54.031 (N(3)CPd6), and +65.636 kcal/mol (N(4)CPc8). In this order, the mean plane deviation of these isomers increased from 0.000 to 0.123, 0.170, 0.215, and 0.251 A, respectively. The unusual tautomeric forms of pyrrole ring with an sp(3)-carbon were found in the stable forms of N(3)CP and N(4)CP. The NICS values at the mean position of the 24 core atoms were nearly the same for the most aromatic isomers regardless of the confusion level: -15.1280 (N(0)CP1), -13.8493 (N(1)CP2), -13.7267 (N(2)CPd1), -11.7723 (N(3)CPb5), and -13.6224 ppm (N(4)CPa6). The positive correlation between aromaticity and stability was inferred from the plots of NICS and the relative energy of NCP for N(0)CP, N(1)CP, and trans-N(2)CP. On the other hand, the correlation was negative for cis-N(2)CP, N(3)CP, and N(4)CP isomers.     

锰(Ⅱ)呋喃甲醛Schiff碱催化苯乙烯环氧化的研究

自1979年Groves首先以金属卟啉模拟细胞色素P－450,实现烯烃的环氧化^[1]以来,仿单加氧酶催化环氧化烯烃就成为仿酶催化领域里的一个非常活跃的研究课题^[2-5],但在这些报道中所用的模型化合物均为金属卟啉及其衍生物或Mn-Salen及其衍生物,这些化合物高昂的价格极大地限制了其应用前景。呋喃甲醛（俗称糠醛）取之于米糠或玉米芯,价格便宜且非石化产品,用它取代水杨醛不仅可降低成本,而且符合绿色化学要求。为此,本文选取了五种锰呋喃甲醛Schiff碱配合物作为模型化合物,以NaOCI为氧化剂,催化苯乙烯环氧化。讨论了配体结构、氧化物的pH值、轴配体、反应时间对催化环氧化反应的影响。     

N,N'-二(芳磺酰) 亚磺酰胺-S-(2-苯并咪唑基) 类化合物的合成

本文报道了新化合物N,N'-二(芳磺酰)亚磺酰胺-S-(2-苯并咪唑基)钠(a～e)以及N,N'-二(芳磺酰)亚磺酰胺-S-(2-苯并咪唑基) (f～i)的合成. 通过在感光乳剂中的应用,我们发现a,b,和c具有超增感作用, 它们分别使卤化银乳剂的感光度提高62％ , 22％ 和 45％.     

N,N′-二(芳磺酰)亚磺酰胺-S-(2-苯并咪唑基)类化合物的合成

本文报道了新化合物N,N＇—二(芳磺酰)亚磺酰胺—S—(2—苯并咪唑基)钠(a～e)以及N,N＇—二(芳磺酰)亚磺酰胺—S—(2—苯并咪唑基)(f～i)的合成。通过在感光乳剂中的应用,我们发现a,b和c具有超增感作用,它们分别使卤化银乳剂的感光度提高62％,22％和45％。 钠—N—氯芳磺酰亚胺化合物既是一类精细化工产品,又是一类重要的反应中间体。由它们     

Synthesis, structure, and electrochemical studies of molybdenum and tungsten dinitrogen, diazenido, and hydrazido complexes that contain aryl-substituted triamidoamine ligands

One-electron reduction of [ArN(3)N]MoCl complexes (Ar = C(6)H(5), 4-FC(6)H(4), 4-t-BuC(6)H(4), 3,5-Me(2)C(6)H(3)) yields complexes of the type [ArN(3)N]Mo-N=N-Mo[ArN(3)N], while two-electron reduction yields ([ArN(3)N]Mo-N=N)(-) derivatives (Ar = C(6)H(5), 4-FC(6)H(4), 4-t-BuC(6)H(4), 3,5-Me(2)C(6)H(3), 3,5-Ph(2)C(6)H(3), and 3,5-(4-t-BuC(6)H(4))(2)C(6)H(3)). Compounds that were crystallographically characterized include ([t-BuC(6)H(4)N(3)N]Mo)(2)(N(2)), Na(THF)(6)([PhN(3)N]Mo-N=N)(2)Na(THF)(3), [t-BuC(6)H(4)N(3)N]Mo-N=N-Na(15-crown-5), and ([Ph(2)C(6)H(3)N(3)N]MoNN)(2)Mg(DME)(2). Compounds of the type [ArN(3)N]Mo-N=N-Mo[ArN(3)N] do not appear to form when Ar = 3,5-Ph(2)C(6)H(3) or 3,5-(4-t-BuC(6)H(4))(2)C(6)H(3), presumably for steric reasons. Treatment of diazenido complexes (e.g., [ArN(3)N]Mo-N=N-Na(THF)(x)) with electrophiles such as Me(3)SiCl or MeOTf yielded [ArN(3)N]Mo-N=NR complexes (R = SiMe(3) or Me). These species react further to yield ([ArN(3)N]Mo-N=NMe(2))(+) species in the presence of methylating agents. Addition of anionic methyl reagents to ([ArN(3)N]Mo-N=NMe(2))(+) species yielded [ArN(3)N]Mo(N=NMe(2))(Me) complexes. Reduction of [4-t-BuC(6)H(4)N(3)N]WCl under dinitrogen leads to a rare ([t-BuC(6)H(4)N(3)N]W)(2)(N(2)) species that can be oxidized by two electrons to give a stable dication (as its BPh(4)(-) salt). Reduction of hydrazido species leads to formation of Mo=N in low yields, and only dimethylamine could be identified among the many products. Electrochemical studies revealed expected trends in oxidation and reduction potentials, but also provided evidence for stable neutral dinitrogen complexes of the type [ArN(3)N]Mo(N(2)) when Ar is a relatively bulky terphenyl substituent.     

Polymorphism and spin crossover in mononuclear Fe(II) species containing new dipyridylamino-substituted s-triazine ligands

Four new dipyridylamino-substituted s-triazine ligands DBB (N(2),N(2),N(4),N(4)-tetrabenzyl-N(6),N(6)-di(pyridin-2-yl)-1,3,5-triazine-2,4,6-triamine), DDB (N(2),N(2),N(4),N(4)-tetrabutyl-N(6),N(6)-di(pyridin-2-yl)-1,3,5-triazine-2,4,6-triamine), DCCl (6-chloro-N(2),N(2)-dicyclohexyl-N(4),N(4)-di(pyridin-2-yl)-1,3,5-triazine-2,4-diamine) and DDT (N(2),N(2),N(4),N(4)-tetraphenyl-N(6),N(6)-di(pyridin-2-yl)-1,3,5-triazine-2,4,6-triamine), have been incorporated into eight new, 0D Fe(II) compounds of type [Fe(II)(NCX)(2)(L)(2)]·Solvent (where NCX = NCS(-), NCSe(-) or N(CN)(2)(-)). The polymorphic compounds α-trans-[Fe(II)(NCS)(2)(DBB)(2)] (1) and β-trans-[Fe(II)(NCS)(2)(DBB)(2)] (2) display, respectively, a relatively abrupt, complete, one-step spin transition with T(?) ~ 170 K, and a more gradual, complete, one-step spin transition with T(?) ~ 300 K. Gradual, one-step spin transitions are observed for trans-[Fe(II)(N(CN)(2))(2)(DBB)(2)]·2CH(3)CH(2)OH (3) and trans-[Fe(II)(NCSe)(2)(DCCl)(2)]·2CH(3)OH (6) with T(?) ~ 280 K for both, while the one-step spin transition observed for a desolvated sample of trans-[Fe(II)(NCSe)(2)(DDB)(2)]·2CH(3)OH (4) is relatively abrupt, showing hysteresis with T(?↑) = 285 K and T(?↓) = 275 K. The compounds cis-[Fe(II)(NCS)(2)(DDB)(2)] (5) and trans-[Fe(II)(NCS)(2)(DDT)(2)]·4CH(2)Cl(2) (7) remain high spin, while structural data on trans-[Fe(II)(NCSe)(2)(DDT)(2)]·4CH(2)Cl(2) (8) suggests a spin transition at low temperatures. It is likely that distortion of the Fe(II)N(6) octahedron, intermolecular interactions and molecular conformation are crucial in deciding both the T(?) and abruptness of the spin transition for these species, although the nature of their influence varies. Variable temperature powder X-ray diffraction measurements on the polymorphs 1 and 2 reveal anisotropy in the unit cell parameters as the spin transition occurs.     

Iodide, azide, and cyanide complexes of (N,C), (N,N), and (N,O) metallacycles of tetra- and pentavalent uranium

In contrast to the neutral macrocycle [UN*(2)(N,C)] (1) [N* = N(SiMe(3))(3); N,C = CH(2)SiMe(2)N(SiMe(3))] which was quite inert toward I(2), the anionic bismetallacycle [NaUN*(N,C)(2)] (2) was readily transformed into the enlarged monometallacycle [UN*(N,N)I] (4) [N,N = (Me(3)Si)NSiMe(2)CH(2)CH(2)SiMe(2)N(SiMe(3))] resulting from C-C coupling of the two CH(2) groups, and [NaUN*(N,O)(2)] (3) [N,O = OC(═CH(2))SiMe(2)N(SiMe(3))], which is devoid of any U-C bond, was oxidized into the U(V) bismetallacycle [Na{UN*(N,O)(2)}(2)(μ-I)] (5). Sodium amalgam reduction of 4 gave the U(III) compound [UN*(N,N)] (6). Addition of MN(3) or MCN to the (N,C), (N,N), and (N,O) metallacycles 1, 4, and 5 led to the formation of the anionic azide or cyanide derivatives M[UN*(2)(N,C)(N(3))] [M = Na, 7a or Na(15-crown-5), 7b], M[UN*(2)(N,C)(CN)] [M = NEt(4), 8a or Na(15-crown-5), 8b or K(18-crown-6), 8c], M[UN*(N,N)(N(3))(2)] [M = Na, 9a or Na(THF)(4), 9b], [NEt(4)][UN*(N,N)(CN)(2)] (10), M[UN*(N,O)(2)(N(3))] [M = Na, 11a or Na(15-crown-5), 11b], M[UN*(N,O)(2)(CN)] [M = NEt(4), 12a or Na(15-crown-5), 12b]. In the presence of excess iodine in THF, the cyanide 12a was converted back into the iodide 5, while the azide 11a was transformed into the neutral U(V) complex [U(N{SiMe(3)}SiMe(2)C{CHI}O)(2)I(THF)] (13). The X-ray crystal structures of 4, 7b, 8a-c, 9b, 10, 12b, and 13 were determined.     

Letter: characterisation and identification of spermine and spermidine derivatives in Microdesmis keayana and Microdesmis puberula roots by electrospray ionisation tandem mass spectrometry and high-performance liquid chromatography/electrospray ionisation tandem mass spectrometry

Three new N(1),N(5),N(14)-tris(4- hydroxycinnamoyl)spermines were identified in hydromethanolic root extracts of Microdesmis keayana J. Léonard and Microdesmis puberula Hook f. The electrospray ionisation tandem mass spectrometry (ESI-MS/MS) technique with specific nuclear magnetic resonance analysis of hydrolysed products made it possible to identify N(1),N(5),N(14)-tris(p-coumaroyl)spermine, N(1)-feruloyl,N(5),N(14)-di(p-coumaroyl)spermine and N(1),N(5),N(14)-tris(feruloyl)spermine, named keayanines B, C and D, respectively. ESI-MS/MS analysis most effectively provided structural data although high-performance liquid chromatography/electrospray ionisation tandem mass spectrometry was also used to characterise four other compounds from Microdesmis puberula-keayanidines A, B, C and keayanine A-which had already been identified in M. keayana. This chemical data is the first to be published for M. puberula which is a commonly used plant in Central African traditional medicine.     

Synthesis and Crystal Structure of 1-[(1-Phenyl-4-cyano)pyrazol-5-yliminomethyl]- 2-nitroiminoimidazolidine

1　INTRODUCTIONNeonicotinoids[1～2]areanovelanddistinctclassofinsecticides.Theycombineselectiveactivityagainstinsectswithafavourablesafetyprofile.Neonicotinoidsactatthenicotinicacetylcholinereceptor(nAChR)[3～4].Sincethefirstneonicotinoid,imi-dacloprid(IMI)1wasintroducedtothemarketbyBayerin1991,alotofitsanalogswerereported.Thesecompoundshavethesamestructuralunit,asshowedindashedlineareainIMI.AccordingtothemodelproposedbyYamamotoetal[5],thedistancebetweenthetwonitrogenatomsofIMIisthe…     

Trimerization of alkali dicyanamides M[N(CN)2] and formation of tricyanomelaminates M3[C6N9] (M = K, Rb) in the melt: crystal structure determination of three polymorphs of K[N(CN)2], two of Rb[N(CN)2], and one of K3[C6N9] and Rb3[C6N9] from X-ray powder diffractometry

The alkali dicyanamides M[N(CN)2] (M=K, Rb) were synthesized through ion exchange, and the corresponding tricyanomelaminates M3[C6N9] were obtained by heating the respective dicyanamides. The thermal behavior of the dicyanamides and their reaction to form the tricyanomelaminates were investigated by temperature-dependent X-ray powder diffractometry and thermoanalytical measurements. Potassium dicyanamide K[N(CN)2] was found to undergo four phase transitions: At 136 degrees C the low-temperature modification alpha-K[N(CN)2] transforms to beta-K[N(CN)2], and at 187degrees C the latter transforms to the high-temperature modification gamma-K[N(CN)2], which melts at 232 degrees C. Above 310 degrees C the dicyanamide ions [N(CN)2]- trimerize and the resulting tricyanomelaminate K3[C6N9] solidifies. Two modifications of rubidium dicyanamide have been identified: Even at -25 degrees C, the a form slowly transforms to beta-Rb[N(CN)2] within weeks. Rb[N(CN)2] has a melting point of 190 degrees C. Above 260 degrees C the dicyanamide ions [N(CN)2]- of the rubidium salt trimerize in the melt and the tricyanomelaminate Rb3[C6N9] solidifies. The crystal structures of all phases were determined by powder diffraction methods and were refined by the Rietveld method. alpha-K[N(CN)2] (Pbcm, a = 836.52(1), b = 46.90(1), c =7 21.27(1) pm, Z = 4), gamma-K[N(CN)2] (Pnma, a = 855.40(3), b = 387.80(1), 1252.73(4) pm, Z = 4), and Rb[N(CN)2] (C2/c, a = 1381.56(2), b = 1000.02(1), c = 1443.28(2) pm, 116.8963(6) degrees, Z = 16) represent new structure types. The crystal structure of beta-K[N(CN)2] (P2(1/n), a = -726.92(1), b 1596.34(2), c = 387.037(5) pm, 111.8782(6) degrees, Z = 4) is similar but not isotypic to the structure of alpha Na[N(CN)2]. alpha-Rb[N(CN)2] (Pbcm, a = 856.09(1), b = 661.711(7), c = 765.067(9) pm, Z = 4) is isotypic with alpha-K[N(CN)2]. The alkali dicyanamides contain the bent planar anion [N(CN)2]- of approximate symmetry C2, (average bond lengths: C-N(bridge) 133, C-N(term) 113 pm; average angles N-C-N 170 degrees, C-N-C 120 degrees). K3[C6N9] (P2(1/c), a = 373.82(1), b = 1192.48(5), c = 2500.4(1) pm, beta = 101.406(3) degrees, Z = 4) and Rb,[C6N9] (P2(1/c), a = 389.93(2), b = 1226.06(6), c = 2547.5(1) pm, 98.741(5) degrees, Z=4) are isotypic and they contain the planar cyclic anion [C6N9]3-. Although structurally related, Na3[C6N9] is not isotypic with the tricyanomelaminates M3[C6N9] (M = K, Rb).     

Synthesis and Crystal Structure of 1,2-Bis(1-phenyl-3-methylthio- 4-iminopyrazolo[3,4-d]pyrimidin-5-yl) ethane

1 INTRODUCTION As purine analogs, pyrzolo[3,4-d]pyrimidines have anti-tumor[1], antibacterial[2] and anti-leukemic activities[3,4]. Few of these, however, have been studied for pesticidal activity. It is reported that some substituted pyrzolo[3,4-d]pyrimidines have good fungicidal activity[5~7]. These prompted us to study pyrazolo[3,4-d]pyrimidines analogs further. It is shown that two possible products can be formed in the reaction of ethyl N-pyrazolylformimidate with alkylamines as sh…     

Synthesis and structural characterization of two-coordinate low-valent 14-group metal complexes bearing bulky bis(amido)silane ligands

A series of germylene, stannylene and plumbylene complexes [η(2)(N,N)-Me(2)Si(DippN)(2)Ge:] (3a), [η(2)(N,N)-Ph(2)Si(DippN)(2)Ge:] (3b), [η(2)(N,N)-Me(2)Si(DippN)(2)Sn:] (4), [η(2)(N,N)-Me(2)Si(DippN)(2)Pb:](2) (5a), and [η(2)(N,N)-Ph(2)Si(DippN)(2)Pb:] (5b) (Dipp = 2,6-iPr(2)C(6)H(3)) bearing bulky bis(amido)silane ligands were readily prepared either by the transamination of M[N(SiMe(3))(2)](2) (M = Sn, Pb) and [Me(2)Si(DippNH)(2)] or by the metathesis reaction of bislithium bis(amido)silane [η(1)(N),η(1)(N)-R(2)Si(DippNLi)(2)] (R = Me, Ph) with the corresponding metal halides GeCl(2)(dioxane), SnCl(2), and PbCl(2), respectively. Preliminary atom-transfer chemistry involving [η(2)(N,N)-Me(2)Si(DippN)(2)Ge:] (3a) with oxygen yielded a dimeric oxo-bridged germanium complex [η(2)(N,N)-Me(2)Si(DippN)(2)Ge(μ-O)](2) (6). All complexes were characterized by (1)H, (13)C, (119)Sn NMR, IR, and elemental analysis. X-ray single crystal diffraction analysis revealed that the metal centres in 3b, 4, and 5b are sterically protected to prevent interaction between the metal centre and the nitrogen donors of adjacent molecules while complex 5a shows a dimeric feature with a strong intermolecular Pb···N interaction.     

Synthesis of N3-substituted uridine and related pyrimidine nucleosides and their antinociceptive effects in mice

Seventy eight N(3)-substituted derivatives of uridine (1), thymidine (2), 2'-deoxyuridine (3), 6-azauridine (4), 2',3'-O-isopropylideneuridine (5), and arabinofuranosyluracil (6) were synthesized and their antinociceptive effects were evaluated. N(3)-(2',4'-Dimethoxyphenacyl)uridine (1l), N(3)-(2',4'-dimethoxyphenacyl)2'-deoxyuridine (3l), and N(3)-(2',5'-dimethoxyphenacyl)arabinofuranosyluracil (6m) possessed 93, 86, and 82% of the antinociceptive effects tested by hot plate, respectively. The antinociceptive effects of three derivatives were 5.8, 5.4, and 5.1-folds of the effect of N(3)-phenacyluridine (1h) (16%), respectively. The structure-activity relationship of N(3)-substituted pyrimidine nucleosides was also discussed.     

Formation of aluminium, aluminium nitride and nitrogen clusters via laser ablation of nano aluminium nitride. Laser Desorption Ionisation and Matrix-Assisted Laser Desorption Ionisation Time-of-Flight Mass Spectrometry

Laser Desorption Ionisation (LDI) and Matrix-Assisted Laser Desorption Ionisation (MALDI) Time-of-Flight Mass Spectrometry (TOFMS) were used to study the pulsed laser ablation of aluminium nitride (AlN) nano powder. The formation of Al(m)(+) (m=1-3), N(n)(+) (n=4, 5), AlN(n)(+) (n=1-5, 19, 21), Al(m)N(+) (m=2-3), Al(3)N(2)(+), Al(9)N(n)(+) (n=5, 7, 9, 11 and 15), Al(11)N(n)(+) (n=4, 6, 10, 12, 19, 21, 23, and 25), and Al(13)N(n)(+) (n=25, 31, 32, 33, 34, 35, and 36) clusters was detected in positive ion mode. Similarly, Al(m)(-) (m=1-3), AlN(n)(-) (n=1-3, 5), Al(m)N(-) (n=2, 3), Al(2)N(n)(-) (n=2-4, 28, 30), N(n)(-) (n=2, 3), Al(4)N(7)(-) Al(8)N(n)(-) (n=1-6), and Al(13)N(n)(-) (n=9, 18, 20, 22, 24, 26, 28, 33, 35, 37, 39, 41 and 43) clusters were observed in negative ion mode. The formation of the stoichiometric Al(10) N(10) cluster was shown to be of low abundance. On the contrary, the laser ablation of nano-AlN led mainly to the formation of nitrogen-rich Al(m)N(n) clusters in both negative and positive ion mode. The stoichiometry of the Al(m)N(n) clusters was determined via isotopic envelope analysis and computer modelling.     

Complexation and back extraction of various metals by water-soluble diglycolamide.

Water-soluble ligands, N,N,N',N'-tetramethyldiglycolamide (TMDGA), N,N,N',N'-tetraethyldiglycolamide (TEDGA), N,N,N',N'-tetrapropyldiglycolamide (TPDGA) and N,N-dipropyldiglycolamic acid (DPDGAc) were prepared and their abilities to complex with and to back-extract the metal cations were investigated. These results indicate that the DGA series and DPDGAc have a stronger complexing ability with Am(III) and Pu(IV) than comparable carboxylic and aminopolycarboxylic acids. Among these ligands, the trend of the strength of their complexing ability is TPDGA approximately TEDGA > TMDGA approximately DPDGAc. TPDGA has significant loss to the extraction solvent due to its high hydrophobicity. It is evident from the present work that TEDGA is the best reagent for the reverse-extraction of not only An(III), (IV) but also Ca(II), Sc(III), Y(III), Zr(IV), La(III), Hf(IV), and Bi(III).     

Mesomorphic behaviour in bent-shaped molecules with side wings at different positions of a central naphthalene core

Six bent-shaped molecules were prepared with central bent cores based on 2,7-, 1,7-, 1,6-, 1,3-, 1,2- and 2,3-dihydroxynaphthalene groups with side wings containing a Schiff's base moiety and dodecyloxy tail, N(2,7), N(1,7), N(1,6), N(1,3), N(1,2) and N(2,3). All of the compounds form fluid smectic mesophases and their mesomorphic behaviour and properties are discussed in terms of their molecular structure. The compounds are categorized into two groups; in one of them, N(2,7), N(1,6) and N(1,3), the bent cores have a bent angle of 120° between the side wings, whereas in the other, N(1,7), N(1,2) and N(2,3), the bent angle is 60°. The typical banana molecule, N(2,7), in the first group, forms a chiral blue phase that shows two distinguishable domains with opposite optical rotations and circular dichroism. Under an electric field, the chiral blue phase is transformed to strongly birefringent B2 phase which possesses a basically homochiral SmC_AP_A structure. N(1,3) also forms a chiral blue phase, but, in contrast, N(1,6), where the side wings are asymmetrically substituted, forms a typical antiferroelectric B2 phase with the racemic SmC_SP_A structure. N(1,2) and N(2,3) of the other group assume a U-like shape to form a conventional SmA phase. Of interest is the fact that N(1,7) forms a chiral blue phase irrespective of having a small bent angle of 60°. This indicates that the distance between side wings as well as the bent angle plays an important role for the formation of banana-shaped smectic phases.     

Synthesis and Crystal Structure of [Copper(1,10-phenanthroline)_2(pyridine)]perchlorates

1 INTRODUCTIONThe molecular structures of five-coordinated copper (II) complexes show an extensive variability ranging from trigonal bipyramidal to square pyramidal stereochemistry, with most complexes displaying a structure which is intermediate between these two extremes[1,2]. Most crystal structures of 1,10-phenanthroline with copper (II) complexes are known, [Cu (phen)2X]Y, where X = Cl, Br, I, CN, NCS, H2O or thiourea and Y = perchlorate, nitrate, tetrafluoroborate, chloride o…     

Komplexe mit N,N,N′,N′-Tetrakis(2-hydroxybenzyl)ethylendiamin (H4tben). Kristallstruktur von Ti(tben)

Complexes with N,N,N′,N′-Tetrakis(2-hydroxybenzyl)ethylenediamine (H₄tben). Crystal Structure of Ti(tben) The complexes of N,N,N′,N′-tetrakis(2-hydroxybenzyl)-ethylenediamine with titanium(IV), vanadium(IV), manganese(IV), and tin(IV) were synthesized and characterized by mass spectrometry. The Mössbauer date were evaluated for the tin compound. The molecular structure of the titanium(IV) complex was determined by X-ray structural analysis, crystallographic data see “Inhaltsübersicht”.     

四(4－N-吡啶基)卟啉衍生物的合成及表征

阳离子卟啉配体;配合物;还原电位;四(4－N-吡啶基)卟啉衍生物的合成及表征     

Synthesis and characterization of silver(I) adducts supported solely by 1,3,5-triazapentadienyl ligands or by triazapentadienyl and other N-donors

Halogenated 1,3,5-triazapentadienyl ligands [N{(C(3)F(7))C(C(6)F(5))N}(2)](-), [N{(CF(3))C(C(6)F(5))N}(2)](-) and [N{(C(3)F(7))C(2,6-Cl(2)C(6)H(3))N}(2)](-), alone or in combination with other N-donors like CH(3)CN, CH(3)(CH(2))(2)CN, and N(C(2)H(5))(3), have been used in the stabilization of thermally stable, two-, three- or four-coordinate silver(i) adducts. X-Ray crystallographic analyses of {[N{(C(3)F(7))C(C(6)F(5))N}(2)]Ag}(n), {[N{(C(3)F(7))C(C(6)F(5))N}(2)]Ag(NCCH(3))}(n), {[N{(C(3)F(7))C(2,6-Cl(2)C(6)H(3))N}(2)]Ag(NCCH(3))}(n), {[N{(CF(3))C(C(6)F(5))N}(2)]Ag(NCCH(3))(2)}(n) and {[N{(C(3)F(7))C(C(6)F(5))N}(2)]Ag(NCC(3)H(7))}(n) revealed the presence of bridging 1,3,5-triazapentadienyl ligands bonded to silver through terminal nitrogen atoms. These adducts are polymeric in the solid state. [N{(C(3)F(7))C(2,6-Cl(2)C(6)H(3))N}(2)]AgN(C(2)H(5))(3) is monomeric and features a 1,3,5-triazapentadienyl ligand bonded to Ag(I) in a κ(1)-fashion via only one of the terminal nitrogen atoms. The solid state structure of [N{(C(3)F(7))C(C(6)F(5))N}(2)]H has also been reported and it forms polymeric chains via inter-molecular N-H···N hydrogen-bonding.