Guanidinium Lactate Ionic Liquid: An Efficient and Recycling Catalyst for Michael Addition Reaction

A facile and efficient 1, 4-conjungate addition（Michael addition） reaction of active methylene compounds to aft-unsaturated compounds, catalyzed by guanidinium lactate ionic liquid（IL9）, has been developed. A range of chalcones and nitroalkenes together with active methylene compounds have been converted smoothly to the corresponding products in high yields.

PHOTOINDUCED ADDITION REACTIONS OF CHLORANIL WITH FURAN DERIVATIVES

Photoinduoed reaction of chloranil （TCBQ） with 2-methylfuran la and 2,5-dimethylfuran 1b in benzene gave addition products 2a and 2b respecvely together with tetrachlorohydroquinone 3. A mechanism of sequential electron and proton transfer from la or 1b to;TCBQ followed by coupling of the furfuryl and semiquinone radical pairs was proposed and is evidenced by the photo-CIDNP studies of the TCBQ-1a and TCBQ-1b systems.

Modification of Nano-alumina Surface by Michael Addition Reaction

A general method for modification of nano-alumina surface is investigated using Michael addition reaction with α,β-unsaturated carbonyl compounds.

Tetramethylguanidium Lactate Ionic Liquid: Catalyst-free Medium for Michael Addition Reaction

A catalyst-free, facile and efficient Michael addition reaction of active methylene compounds as well as nitromethane with chalcones catalyzed by guanidinium lactate ionic liquid was done. A series of chalcones, nitromethane, and active methylene compounds were converted smoothly to the corresponding products in high yields. The simple procedure, very mild conditions, high yields, and reuse of the IL without any loss of catalytic activity make this protocol considerably attractive for academic researches and practical applications.

Nickel (Ⅱ) Complex Catalyzed Conjugate Addition Reaction of Functionalized Organozinc Reagents to α,β-Unsaturated Esters

Functionalized organozinc reagents can easily under 1, 4-addition reaction withunsaturated esters in the presence of catalytic amount of Ni (acac)_2 and tertiary ammes under verymild conditions to give the products in excellent yields.

Theoretical Study on the Addition Reactions of Benzaldoximes with Propene

The Michael addition reactions of Z and E benzaldoximes with propene were investigated theoretically by DFT method at B3LYP/6-31G^＊ level. The calculation results show that both addition reactions are concerted processes accompanied by the migration of hydrogen from the atom oxygen to carbon. Both products Z and E nitrones have dipolar charge distributions and activities. Z isomer is more favorable in the reaction due to the barrier is lower.

Addition Reaction of Fe(CO)_n (n = 3～5) on Fullerene C_(50), C_(60), and C_(70): A Density Functional Theory Study

The electronic structure and reactivities of Fe（CO）n （n = 3~5） addition to different fullerenes have been investigated through the first-principles calculations, and the results indicate that Fe（CO）3 and Fe（CO）4 can be adsorbed to the outside network of fullerene via hollow and bridge sites, respectively. Both of them have larger binding energy, but when Fe（CO）5 is adsorbed via the top site, the binding energy is relatively smaller. According to the directional curvature theory, the reactivities of Fe（CO）3 addition to the fullerenes are determined by KM of the ring center, and those of Fe（CO）4 addition by KD of the C–C bond curvature; while for Fe（CO）5, it presents weak reactivities in the addition reaction because of the larger volume effect. No matter whether the addition reaction takes place on the hollow or bridge site, the binding energies show a linear relationship with KD. This work further enriched the directional curvature theory and applied the isolobel analogy theory in the fullerene addition reactions.

The Addition Reaction of p-Chlorobenzaldoxime Dehydrodimer with 1,3-Dienes

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CAN TRICHLOROMETHANE SULFONYL BROMIDE BE USED AS AN ADDENDUM AS WELL AS A TELOGEN IN ITS ADDITION REACTION T0 VINYLIDENE FLUORIDE?

CCl_3SO_2Br used as a 'telogen' reacts with CH_2=CF_2 to give mainly the 'mono- adduct' CCl_3CH_2CF_2Br, together with very small amouats of CCl_3CF_2CH_2Br, CCl_2BrCH_2CF_2Br and the 'di-adduct' CCl_3(CH_2CF_2)_2Br. The result indicates that CCl_3SO_2Br can be used as an addendum in trichloromethyl-bromo-addition reactions to olefins.

Addition Reaction of Bis(diphenylphosphinyl) Butadiyne with Methylcyclopentadiene

Bis（diphenylphosphinyl）butadiyne reacted with methylcyclopentadiene at room temperature and four isomeric products were obtained. Crystal structures of isomers 1 and 3 have been determined. Crystal data for compound 1 C40H36O2P2·2CHCl3： monoclinic, space group C12/c1 with a = 17.983（2）, b = 11.8723（12）, c = 20.081（2） A, β = 111.218（3）°, V= 3996.5（8） A^3, Z = 4, Mr= 849.36, Dc = 1.412 g/cm^3, F（000） = 1752,μ = 0.546 mm^-1, the final R = 0.0351 and wR = 0.0951 for 3965 observed reflections （I 〉 2σ（I））; and those for compound 3 C40H36O2P2·H2O： triclinic, space group PI with a = 10.4144（15）, b = 13.0558（18）, c = 13.742（2） A, a = 70.453（8）, β = 75.382（8）, γ = 72.312（8）°, V = 1653.7（4） A^3, Z = 2, Mr= 628.64, Dc = 1.262 g/cm^3, F（000） = 664,μ = 0.169 mm^-1, the final R = 0.0593 and wR = 0.1296 for 4891 observed reflections （I 〉 2σ（I））. The structures of the other two isomers are identified via IR, ^1H NMR and MS spectra.

Conjugate Addition Reactions of Functionalized Organozinc-copper Reagents to α,β-Unsaturated Esters

Functionalized organozinc reagents can easily conduct 1,4-addition reaction with unsaturated esters in the presence of Cu(OAc)2 and LiCl under very Anld conditions to give the products in excellent yields.

Organophosphine bearing multiple hydrogen-bond donors for asymmetric Michael addition reaction of 1-oxoindane-2-carboxylic acid ester via dual-reagent catalysis

Multiple hydrogen bonds containing nucleophilic phosphines derived from dipeptide dual-reagents catalyzed asymmetric Michael addition reactions between indene esters and activated olefins in high yields and good to excellent enantioselectivities under mild reaction conditions.The success of current highly selective reactions should provide inspiration for expansion to other reactions and would open up new paradigms for the synthesis of indanone derivatives bearing chiral quaternary carbon centers.

Reconfiguring perovskite interface via R4NBr addition reaction toward efficient and stable FAPbI3-based solar cells

Defect states in perovskite films restrict the interfacial stability and open-circuit voltage of perovskite solar cells.Here,aiming at superior interfacial passivation,we investigate the reconfiguration of perovskite interface by the interaction between a series of quaternary ammonium bromides(QAB)and lead—halide(Pb—X)octahedrons.Bromide—iodide substitution reaction or R4NBr addition reaction may occur on the perovskite surface,which is related to the steric hindrance of quaternary ammonium cations.On this basis,the perovskite surface morphology,band structure,growth orientation and defect states are reconstructed via the R4NBr addition reaction.This ordered lead—halide adduct could effectively repair the imperfect perovskite/hole transportation layer interface to suppress non-radiative recombination and ion migration toward ultralong carrier lifetime surpassing 10µs.The resulting perovskite solar cells yield the efficiency of 23.89%with steady-state efficiency of 23.70%.The passivated cells can sustain 86%of initial efficiency after 200-h operation,which is attributed to the passivation effect and hydrophobic characteristics.This work provides an avenue for reconfiguring perovskite surface by QABs.

Michael Addition Reaction of Fluorinated Nitro Compounds

The Michael addition reactions of fluorinated nitro compounds with electron deficient olefins to give γ-fiuoro-γ-nitro-esters, nitriles and ketones which bear a fluorinated quaternary carbon center were reported. The reactions were promoted by TMG, affording the desired adducts in acceptable to good yields.

Regioselective synthesis of linalyl compounds via addition reaction of geranyl bromide and tin with carbonyl compounds

Linalyl alkyl or aryl carbinols were regioselectively synthesized by the reaction of geranyl bromide and powdered tin with aldehydes and ketones.

Addition Reactivity of C_(36) Cage Controlled by the Curvature and the Electronic Factors:A DFT Study

The molecular geometries and electronic structures of the fullerene derivatives C36（OH）n（n = 1～2） have been investigated on the basis of density functional theory calculation at the B3LYP/6-31＋＋G＊ level.The geometry optimization results indicate that the location of C2 atom is the most active site in the three potential adding patterns,and the C1 or C2 site has a larger binding energy than C3 for the addition reactions of C36（D6h） cage and OH radicals resulting from the larger curvature.The electronic structure calculation results disclose that the C2 site has larger electronic population in HOMO and larger spin density,and the addition reaction on the C2 site need overcome a lesser energy gap than that on the C1 or C3 site.Thus,the addition is controlled jointly by the curvature and the electronic factors.Besides,when two hydroxyls are added to the C36 surface,the C2 sites are also the most active locations.The most stable addition adduct of C36（OH）2 is the isomer which holds Ci symmetry,and the spin multiplicity seriously affects the stabilities of the adducts.

Anion cascade reactions Ⅲ:Synthesis of 3-isoquinuclidone bridged polycyclic lactams

Bridged polycyclic lactams are important structural units in organic functional materials,natural products,and pharmaceuticals.A flexible and efficient anion cascade reaction was developed for the preparation of bridged polycyclic lactams from readily available malonamides and 1,4‑dien-3-ones.Various highly substituted bridged polycyclic lactams were synthesized in good to excellent yields by tandem nucleophilic sequences in the presence of t BuOK in commercially available EtOH solvent at 60℃.Notably,the simple reactions can be run on a gram scale.Mechanistically,bis-Michael addition reaction and hemiaminalization reactions are involved in the tandem transformation.

Density Functional Theory Studies on the Mechanism of Activation Formic Acid Catalyzed by Transition Metal Oxide MoO

This paper systematically studies the reaction mechanisms of formic acid catalyzed by transition metal oxide MoO. Three different reaction pathways of Routes I, Ⅱ and Ⅲ were found through studying the reaction mechanism of transition metal oxide MoO catalyzing the formic acid. The transition metal oxide MoO interacts with the C=O double bond to form chiral chain compounds（Routes I and Ⅱ） and metallic compound MoOH2（Route Ⅲ）. In this paper, we have studied the mechanisms of two addition reaction pathways and hydrogen abstraction reaction pathway. Routes I and Ⅱ are both addition reactions, and their products are two different chiral compounds MoO3CH2, which are enantiomeric to each other. In Route Ⅲ, metal compounds MoOH2 and CO2 are obtained from the hydrogen abstraction reaction. Among them, the hydrogen abstraction reaction occurring in Route Ⅲ is more likely to occur than the others. By comparing the results of previous studies on the reaction of MxOy-＋ ROH（M= Mo,W; R = Me, Et）, we found that the hydrogen abstraction mechanism is completely different from the mechanism of oxygen-containing organic compound catalyzed by MxOy.

A Facile Synthesis of 0,0-Dialkyl-α-(Phenyl Carbamyloxy) Alkyl Phosphonates

A series of title compounds were synthesized by the addition reaction of dialkyl-α-hydroxyphosphonates and phenyl isocyanate under base catalysis. All new compounds have beenidentified by 1H NMR, 31P NMR, IR and elemental analysis.

Microwave-assisted synthesis of diaryl or aryl-alkyl sulfones without catalyst

The microwave-assisted coupling reaction of electrondeficient aryl halides with sulfinic acid salts through SNAr-based addition reactions within 5-30 min. No catalysts were required under our conditions.