N‐Functionalized Ferrocenes: Subvalent Group XIV Element Chlorides and tert‐Butyllithium‐Induced C−C Bond Cleavage under Mild Conditions

The ferrocene derivative (η⁵‐Cp)Fe{η⁵‐C₅H₃‐1‐(ArNCH)‐2‐(CH₂NMe₂)} ( 1 ; Ar=2,6‐iPr₂C₆H₃)) reacts diastereoselectively with LiR by carbolithiation and subsequent hydrolysis to give (η⁵‐Cp)Fe{η⁵‐C₅H₃‐1‐(ArHNCHR)‐2‐(CH₂NMe₂)} ( 3 : R=tBu; 4 : R=Ph; 5 : R=Me) in high yields. For R=tBu, the organolithium derivative (η⁵‐Cp)Fe{η⁵‐C₅H₃‐1‐(ArLiNCHR)‐2‐(CH₂NMe₂)} ( 2 ) was isolated. Compound 2 reacts with GeCl₂?dioxane and SnCl₂ to give the metallylene amide chlorides (η⁵‐Cp)Fe{η⁵‐C₅H₃‐1‐(ArMNCHtBu)‐2‐(CH₂NMe₂)} 6 (M=GeCl) and 7 (M=SnCl), respectively, which each contain three stereogenic centers. The potential of 7 as a ligand in transition‐metal chemistry is demonstrated by formation of its complex (η⁵‐Cp)Fe{η⁵‐C₅H₃‐1‐(ArMNCHtBu)‐2‐(CH₂NMe₂)} [ 9 , M= Sn(Cl)W(CO)₅]. Treatment of 3 with tert‐butyllithium at room temperature causes an unprecedented carbon–carbon bond cleavage whereas under kinetic control, lithiation at the Cp‐3 position takes place, which leads to the isolation of (η⁵‐Cp)Fe{η⁵‐C₅H₃‐1‐(ArHNCHtBu)‐2‐(CH₂NMe₂)‐3‐SiMe₃} ( 10 ).     

Densité des vecteurs propres généralisés d'une classe d'opérateurs compacts non auto-adjoints et applications

We consider a closed densely defined linear operatorT in a Hilbert spaceE, and assume the existence of ₀ (T) such thatK = (T - ₀ I)^-1 is compact and the existence ofp>0 such thats _n (K)=o((n ^–1/p)), whereS _n (K) denotes the sequence of non-zero eigenvalues of the compact hermitian operator . In this work, sufficient conditions (announced in [1]) are introduced to assure that the closed subspace ofE spanned by the generalized eigenvectors ofT coincides withE. These conditions are in particular verified by a family of non-self-adjoint operators arising in reggeon's field theory.     

Etude spectrale d'une famille d'opérateurs non-symétriques intervenant dans la théorie des champs de reggeons

In this paper, we study a few spectral properties of a non-symmetrical operator arising in the Gribov theory. The first and second section are devoted to Bargmann's representation and the study of general spectral properties of the operator: $$\begin{gathered} H_{\lambda ',\mu ,\lambda ,\alpha } = \lambda '\sum\limits_{j = 1}^N {A_j^{ * 2} A_j^2 + \mu \sum\limits_{j = 1}^N {A_j^ * A_j + i\lambda \sum\limits_{j = 1}^N {A_j^ * (A_j + A_j^ * )A_j } } } \hfill \\ + \alpha \sum\limits_{j = 1}^{N - 1} {(A_{j + 1}^ * A_j + A_j^ * A_{j + 1} ),} \hfill \\ \end{gathered}$$ whereA* _j andA _j ,j∈[1,N] are the creation and annihilation operators. In the third section, we restrict our study to the case of nul transverse dimension (N=1). Following the study done in [1], we consider the operator: $$H_{\lambda ',\mu ,\lambda } = \lambda 'A^{ * 2} A^2 + \mu A^ * A + i\lambda A^ * (A + A^ * )A,$$ whereA* andA are the creation and annihilation operators. For λ′>0 and λ′²≦μλ′+λ². We prove that the solutions of the equationu′(t)+H _{λ′, μ,λ} u(t)=0 are expandable in series of the eigenvectors ofH _λ′,μ,λ fort>0. In the last section, we show that the smallest eigenvalue σ(α) of the operatorH _{λ′,μ,λ,α} is analytic in α, and thus admits an expansion: σ(α)=σ₀+ασ₁+α²σ₂+..., where σ₀ is the smallest eigenvalue of the operatorH _{λ′,μ,λ,0}.     

The Effect of Combining Post-Harvest Calcium Nanoparticles with a Salicylic Acid Treatment on Cucumber Tissue Breakdown via Enzyme Activity during Shelf Life

In the present study, an experiment was carried out on the postharvest of cucumber fruit during a 14-day shelf life. The aim was to assess the impact of calcium nanoparticles (CaNPs) blended with different concentrations of salicylic acid (SA) on the shelf life of cucumbers during the seasons of 2018 and 2019. The investigation further monitored the influences of CaNPs-SA on some physical properties of cucumber, including the percentage weight loss, color, and fruit firmness. In addition, chemical properties, such as total soluble solids (SSC%), total acidity (TA%), total soluble sugars, and chlorophyll pigmentation of the fruit skin, were assessed during a 14-day shelf lifeCell wall degradation enzymes (CWEAs) such as polygalacturonase (PG), cel-lulase (CEL), xylanase (XYL), and pectinase (PT) were also researched. In addition, the generation rates of H₂O₂ and O₂^•− were calculated, as well as the reduction of DPPH. The lipid peroxidation (malondialdehyde, MDA) and cell membrane permeability (IL%) of cell wall composites were also determined. CaNPs-SA at 2 mM suppressed CWEAs, preserved fruit quality, reduced weight loss throughout the shelf-life period, and reduced the percent leakage value. At this concentration, we also found the lowest levels of MDA and the highest levels of DPPH.     

Cycloaddition reactions in aqueous systems: A two-decade trend endeavor

Cycloaddition reactions are an integral and weighty part of organic chemistry in pedagogy and research as well. The wealthy literature on cycloaddition reactions from their birth up to now, unequivocally witnesses to their leading chemistry. The so-called “conventional solvents” are organic solvents that have indubitably promoted their success. Yet, the toxicity facet of these solvents impedes their use freely and with no fear. Not only is the operating chemist uncomfortable while experimenting, but also the environment is equally threatened. Working out the cycloaddition reactions and other organic ones in aqueous systems would certainly bring some relief to the chemist and to the environment as well. Unusual outcomes in terms of yield, reactivity and selectivity compared to those performed in organic solvents were commonly observed, and have overwhelmed the chemists with surprise indeed. In this review, homo Diels–Alder reactions in aqueous media include those involving the following dienophiles: maleimides, α,β-unsaturated esters, p-benzoquinones, vinyl ketones, phenyl-1-(2-pyridyl)-2-propen-1-one, α,β-unsaturated esters. A special case is the organocatalysis of Diels–Alder cycloaddition of α,β-unsaturated ketones (aldehydes). Of no less importance, some hetero Diels–Alder cycloaddition reactions in water systems are delineated. The impact of additives (salts, organic and inorganic chemicals), micellar catalysis and Lewis/Brønstëd acid catalysis on outcomes of such cycloaddition reactions is discussed. The 1,3-dipolar cycloaddition methodology applied to aqueous media has brought forth a number of heterocyclic compounds, usually with a regio- and stereoselectivity pecularity. These heterocycles include triazoles, tetrazoles, pyrazoles, isoxazoles, isoxazolidines, pyrroles and pyrrolidines. The superiority of copper(I) catalysis in the azide-alkyne cycloaddition (Huisgen cycloaddition) in water is endorsed by a number of examples.     

The influence of adding marble and granite dust on the mechanical and physical properties of PP composites

Journal of Thermal Analysis and Calorimetry - The purpose of this work is to investigate the opportunity of re-using M&G wastes to get novel PP composites. Recycling of marble and granite...     

Competitive adsorption of anionic dyes onto DMOA modified MCM-41

Research on Chemical Intermediates - The single and binary adsorption of two anionic dyes Acid Yellow 17 (AY17) and Naphtol Green B (NGB) onto N–N–Dimethyl-n-octylamine (DMOA) modified...