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81.
Frik M Jiménez J Gracia I Falvello LR Abi-Habib S Suriel K Muth TR Contel M 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(12):3659-3674
The reaction of new dinuclear gold(I) organometallic complexes containing mesityl ligands and bridging bidentate phosphanes [Au(2)(mes)(2)(μ-LL)] (LL=dppe: 1,2-bis(diphenylphosphano)ethane 1a, and water-soluble dppy: 1,2-bis(di-3-pyridylphosphano)ethane 1b) with Ag(+) and Cu(+) lead to the formation of a family of heterometallic clusters with mesityl bridging ligands of the general formula [Au(2)M(μ-mes)(2) (μ-LL)][A] (M=Ag, A=ClO(4)(-), LL=dppe 2a, dppy 2b; M=Ag, A=SO(3)CF(3)(-), LL=dppe 3a, dppy 3b; M=Cu, A=PF(6)(-), LL=dppe 4a, dppy 4b). The new compounds were characterized by different spectroscopic techniques and mass spectrometry The crystal structures of [Au(2)(mes)(2)(μ-dppy)] (1b) and [Au(2)Ag(μ-mes)(2)(μ-dppe)][SO(3)CF(3)] (3a) were determined by a single-crystal X-ray diffraction study. 3a in solid state is not a cyclic trinuclear Au(2)Ag derivative but it gives an open polymeric structure instead, with the {Au(2)(μ-dppe)} fragments "linked" by {Ag(μ-mes)(2)} units. The very short distances of 2.7559(6)?? (Au-Ag) and 2.9229(8)?? (Au-Au) are indicative of gold-silver (metallophilic) and aurophilic interactions. A systematic study of their luminescence properties revealed that all compounds are brightly luminescent in solid state, at room temperature (RT) and at 77?K, or in frozen DMSO solutions with lifetimes in the microsecond range and probably due to the self-aggregation of [Au(2)M(μ-mes)(2)(μ-LL)](+) units (M=Ag or Cu; LL=dppe or dppy) into an extended chain structure, through Au-Au and/or Au-M metallophilic interactions, as that observed for 3a. In solid state the heterometallic Au(2)M complexes with dppe (2a-4a) show a shift of emission maxima (from ca. 430 to the range of 520-540?nm) as compared to the parent dinuclear organometallic product 1a while the complexes with dppy (2b-4b) display a more moderate shift (505 for 1b to a max of 563?nm for 4b). More importantly, compound [Au(2)Ag(μ-mes)(2)(μ-dppy)]ClO(4) (2b) resulted luminescent in diluted DMSO solution at room temperature. Previously reported compound [Au(2)Cl(2)(μ-LL)] (LL dppy 5b) was also studied for comparative purposes. The antimicrobial activity of 1-5 and Ag[A] (A=ClO(4)(-), SO(3)CF(3)(-)) against gram-positive and gram-negative bacteria and yeast was evaluated. Most tested compounds displayed moderate to high antibacterial activity while heteronuclear Au(2)M derivatives with dppe (2a-4a) were the more active (minimum inhibitory concentration 10 to 1?μg?mL(-1)). Compounds containing silver were ten times more active to gram-negative bacteria than the parent dinuclear compound 1a or silver salts. Au(2)Ag compounds with dppy (2b, 3b) were also potent against fungi. 相似文献
82.
Josefina T. Hamutoko Heike Wanke Paul Koeniger Matthias Beyer Marcel Gaj 《Isotopes in environmental and health studies》2017,53(4):382-399
A hydrogeochemical and stable isotope study (2H and 18O) was carried out in the Cuvelai-Etosha Basin in order to characterize available groundwater and to identify possible recharge mechanisms for the perched aquifers. Data were collected during seven field campaigns between 2013 and 2015 from a total of 24 shallow and deep groundwater hand-dug wells. In the investigated groundwaters, hydrogencarbonate is the dominating anion in both well types, whereas cations vary between calcium and magnesium in deep wells, and sodium and potassium in shallow wells. Groundwater chemistry is controlled by dissolution of carbonate minerals, silicate weathering and ion exchange. Stable isotopic composition suggests that deep groundwater is recharged by high-intensity/large rainfall events, whereas the shallow wells can even be recharged by less-intense/small rainfall events. Water in deep wells reflect a mixture of water influenced by evaporation during or before infiltration and water that infiltrated through fast preferential pathways, whereas shallow wells are strongly influenced by evaporation. The findings of this research contribute to improve the understanding of hydrogeochemistry, recharge paths and temporal variations of perched aquifers. 相似文献
83.
Ana Sofía Lemus de la Cruz Josefina Barrera-Corts Laura Patricia Lina-García Ana C. Ramos-Valdivia Rosa Santilln 《Molecules (Basel, Switzerland)》2022,27(9)
Cedrela odorata L. is a plant species from the Meliaceae family that is cultivated for timber production. Although the C. odorata essential oil (EO) contains mainly sesquiterpenes, its insecticidal potential is unknown. The lipophilic properties and high degradation capacity of EOs have limited their application for use in pest control. However, the currently available knowledge on the nanoemulsification of EOs, in addition to the possibility of improving their dispersion, would allow them to prolong their permanence in the field. The objective of the present work was to develop a nanoemulsion of the C. odorata EO and to evaluate its larvicidal activity against Spodoptera frugiperda. The EO was obtained by the hydrodistillation of C. odorata dehydrated leaves, and the nanoemulsion was prepared with non-ionic surfactants (Tween 80 and Span 80) using a combined method of agitation and dispersion with ultrasound. The stability of the nanoemulsion with a droplet diameter of <200 nm was verified in samples stored at 5 °C and 25 °C for 90 days. Both the C. odorata EO and its corresponding nanoemulsion presented lethal properties against S. frugiperda. The results obtained provide guidelines for the use of wood waste to produce sustainable and effective insecticides in the fight against S. frugiperda. In addition, considering that a phytochemical complex mixture allows the simultaneous activation of different action mechanisms, the development of resistance in insects is slower. 相似文献
84.
Pablo Ríos Dr. Josefina Díez Dr. Joaquín López‐Serrano Dr. Amor Rodríguez Dr. Salvador Conejero 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(47):16791-16795
The low‐electron‐count cationic platinum complex [Pt(ItBu’)(ItBu)][BArF], 1 , interacts with primary and secondary silanes to form the corresponding σ‐SiH complexes. According to DFT calculations, the most stable coordination mode is the uncommon η1‐SiH. The reaction of 1 with Et2SiH2 leads to the X‐ray structurally characterized 14‐electron PtII species [Pt(SiEt2H)(ItBu)2][BArF], 2 , which is stabilized by an agostic interaction. Complexes 1 , 2 , and the hydride [Pt(H)(ItBu)2][BArF], 3 , catalyze the hydrosilation of CO2, leading to the exclusive formation of the corresponding silyl formates at room temperature. 相似文献
85.
Marc Rudolf Olga Trukhina Josefina Perles Lai Feng Takeshi Akasaka Tomas Torres Dirk M. Guldi 《Chemical science》2015,6(7):4141-4147
Two subphthalocyanine–C60 conjugates have been prepared by means of the 1,3-dipolar cycloaddition reaction of (perfluoro) or hexa(pentylsulfonyl) electron deficient subphthalocyanines to C60. Comprehensive assays regarding the electronic features – in the ground and excited state – of the resulting conjugates revealed energy and electron transfer processes upon photoexcitation. Most important is the unambiguous evidence – in terms of time-resolved spectroscopy – of an ultrafast oxidative electron transfer evolving from C60 to the photoexcited subphthalocyanines. This is, to the best of our knowledge, the first case of an intramolecular oxidation of C60 within electron donor–acceptor conjugates by means of only photoexcitation. 相似文献
86.
A method for constructing projectively unique polytopes with many vertices is described. The method makes use of the properties of Gale diagrams. 相似文献
87.
Josefina Alvarez 《Journal d'Analyse Mathématique》1994,62(1):155-167
The direct proof by R. R. Coifman and Y. Meyer of theT(1) Theorem of G. David and J. L. Journé is based on the following result.
LetT be an operator associated to a kernelk(x, y) satisfying
相似文献
88.
alpha-Amino selenoester-tethered electronically poor alkenes on treatment with tributyltin hydride or TTMSS undergo intramolecular radical cyclization to provide 6-azabicyclo[3.2.1]octanes through 1-aminomethyl radical intermediates. 相似文献
89.
Cadierno V Díez J García-Garrido SE Gimeno J 《Chemical communications (Cambridge, England)》2004,(23):2716-2717
The 16e(-) derivative [Ru(eta3-2-C3H4Me)(CO)(dppf)][SbF6] catalyzes: (i) the propargylic substitution reaction of 1,1-diphenyl-2-propyn-1-ol with alcohols to produce propargylic ethers, and (ii) the formal isomerization of 1,1-diphenyl-2-propyn-1-ol into 3,3-diphenyl-2-propenal. 相似文献
90.
Cristian A. Strassert Josefina Awruch 《Monatshefte für Chemie / Chemical Monthly》2006,83(3):1499-1503
Reduction of N-alkylsubstituted phthalimides to the corresponding isoindolines by means of diborane is herein described. 相似文献
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