具有荧光响应功能的分子四边形的组装(英文)

由缩氨基脲和2-喹啉醛合成了席夫碱配体H2L,并与过渡金属离子Cd2+组装得到了四边形配合物CQ。用X射线衍射对配合物的晶体结构进行了测定,发现其具有I41/a空间群。通过荧光测试发现该配合物在CH3CN溶液中具有较强的荧光,加入间苯二甲酸、对苯二甲酸阴离子后荧光发生淬灭,而加入邻苯二甲酸阴离子荧光无变化,可以将邻苯二甲酸阴离子从其他2种二酸阴离子中区分出来。     

Synthesis of Dialkyl 2‐(Alkylamino)‐4,9‐dihydro‐9‐oxocyclohepta[b]pyran‐3,4‐dicarboxylates

Dialkyl 2‐(alkylamino)‐4,9‐dihydro‐9‐oxocyclohepta[b]pyran‐3,4‐dicarboxylates are prepared in a one‐pot three‐component reaction of alkyl isocyanide, dialkyl acetylenedicarboxylate, and α‐tropolone (=2‐hydroxycyclohepta‐2,4,6‐trienone). The reaction proceeds smoothly at room temperature and under neutral conditions to afford tropolone derivatives in high yield.     

Organothallium compounds. Mechanistic study of the disproportionation reaction of organothallium compounds with copper in acetonitrile

Disproportionation reactions of various phenyl- and thienylthallium dicarboxylates with copper in acetonitrile have been carried out. The reaction mechanism proposed involves the participation of the ArTl²⁺ dication and various cationic pairs of the dication and the intermediate formation of organothallium radicals.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 1970–1973, November, 1993.     

Variable temperature Mössbauer spectroscopic studies of oxo-centered trinuclear mixed-valence iron succinate, mesaconate and isophthalate complexes

Three new oxo-centered trinuclear mixed-valence iron complexes, iron succinate, iron mesaconate and iron isophthalate have been prepared. Temperature dependent valence delocalization processes were observed for all the complexes on variable temperature Mössbauer spectroscopic studies. Two clear quadrupole split doublets attributed to high-spin Fe(III) and high-spin Fe(II) states were existed for the complexes at liquid nitrogen temperature. At room temperature a nearly averaged singlet peak was observed for mesaconate complex and averaged doublet peaks were observed for succinate and isophthalate complexes with IS values 0.68 and 0.68 mms^?1 and QS values 0.44 and 0.48 mms^?1 respectively.     

An expedient synthesis of spirooxindoles incorporating 2-amino pyran-3-carbonitrile unit employing dialkyl acetone-1,3-dicarboxylates

Spirooxindoles are a class of molecules possessing significant biological effects such as antiviral, antifungal, antibacterial and anticancer properties. Herein we report a series of spirooxindole molecules having 2-amino pyran-3-carbonitrile and with two ester groups. These molecules were prepared by the reaction of dialkyl acetone-1,3-dicarboxylate and isatilidenes in the presence of triethyl amine.     

Structural study of di- and triorganotin(IV) dicarboxylates containing one double bond

Tri- and diorganotin(IV) dicarboxylates derived from trans-glutaconic acid and acetone 1,3-dicarboxylic acid were prepared. Their structure was studied using NMR, IR, and MS data. All of these compounds (except for compound 2a) are polymeric in the solid state and depolymerise upon dissolving in deuteriochloroform to give monomeric particles with four-coordinated central tin atoms. X-ray crystallography was used to characterize (E)-bis(tributylstannyl) pent-2-enedioate (1a). This compound crystallizes in a monoclinic space group system. The supramolecular organization of 1a can be described as layered polymeric sheets constructed of forty-membered rings that are interconnected on four different sites to the third dimension. Each layer assembled of the forty-membered rings, is made up of six triorganotin fragments and six trans-glutaconic acids, where four of them are incorporated in the core of the ring and other two are bidentate bridging and participating in the ring system by three atoms of CO₂ group only.     

One‐Pot Synthesis of Novel Pyrrolo[1,2‐a]quinoxaline‐4(5H)‐ones Using Benzene‐1,2‐diamine,Acetylenedicarboxylates, and β‐Nitrostyrene Derivatives

The reaction between a variety of o‐phenylenediamines (=benzene‐1,2‐diamines), dialkyl acetylenedicarboxylates, and derivatives of nitrostyrene (=(E)‐(2‐nitroethenyl)benzene) in the presence of sulfamic acid (SA; H₃NSO₃) as catalyst led to the corresponding pyrrolo[1,2‐a]quinoxaline‐4(5H)‐one derivatives in high yields.     

Condensation of 4-chloro-2H-chromene-3-carbaldehydes and ethyl-3-aminocrotonates with p-TsOH: a facile approach for the synthesis of chromenyldihydropyridines

The investigated reaction of 4-chloro-2H-chromene-3-carbaldehyde 1a with ethyl 3-oxobutanoate 2a in the presence of ammonium acetate provided two compounds, 2H-chromenyldihydropyridine dicarboxylate 3a and chromenopyridine carboxylate 4a. However, the reaction of 1a with ethyl-3-aminocrotonate 5a in the presence of p-TsOH provided selectively 2H-chromenyldihydropyridine dicarboxylate 3a with very good yield. The established method was applied for the preparation of series of 2H-chromenyldihydropyridine dicarboxylates 3a–q.     

One‐Pot Four‐Component Synthesis of Tetrasubstituted Pyrroles

A convenient one‐pot four‐component synthesis of tetrasubstituted pyrroles was carried out through the reaction of butane‐2,3‐dione with α‐aminophosphorous ylides, obtained in situ from the 1 : 1 : 1 addition reaction between triphenylphosphine, dialkyl acetylenedicarboxylate, and ammonium acetate.     

Formation of Dialkyl 2‐[3‐Alkoxy‐1‐(alkylimino)‐1‐chloro‐3‐oxopropan‐2‐ylidene]hydrazine‐1,1‐dicarboxylates of α‐(Alkoxycarbonyl)imidoyl Chlorides from PhosphineDiazo Ester Zwitterions and Nef‐Isocyanide Adducts

A novel transformation involving phosphine? diazo ester zwitterions (generated from dialkyl azodicarboxylates with Ph₃P) and α‐(alkoxycarbonyl)imidoyl chlorides (prepared from α‐addition of acyl chlorides to alkyl isocyanides) to afford dialkyl 2‐[3‐alkoxy‐1‐(alkylimino)‐1‐chloro‐3‐oxopropan‐2‐ylidene]hydrazine‐1,1‐dicarboxylates in moderate yields, is described.