Pyridinesilver Tetraoxometallate Complexes: Overview of the Synthesis, Structure, and Properties of Pyridine Complexed AgXO4 (X = Cl, Mn, Re) Compounds

We reviewed the synthesis, structure, and properties of pyridine complexes of AgXO4 (X = Cl, Mn, and Re) compounds with various compositions ([AgPy2] XO4, [AgPy2XO4]·0.5Py, [AgPy4] XO4, and 4 [AgPy2XO4] [AgPy4] XO4). We also clarified the controversial information about the existence and composition of pyridine complexes of silver permanganate, used widely as mild and selective oxidants in organic chemistry. We discussed in detail the available structural and spectroscopic (IR, Raman, and UV) data and thermal behavior, including the existence and consequence of quasi-intramolecular reactions between the reducing ligand and anions containing oxygen.

Recent Progress in Metal-Catalyzed [2+2+2] Cycloaddition Reactions

Metal-catalyzed [2+2+2] cycloaddition is a powerful tool that allows rapid construction of functionalized 6-membered carbo- and heterocycles in a single step through an atom-economical process with high functional group tolerance. The reaction is usually regio- and chemoselective although selectivity issues can still be challenging for intermolecular reactions involving the cross-[2+2+2] cycloaddition of two or three different alkynes and various strategies have been developed to attain high selectivities. Furthermore, enantioselective [2+2+2] cycloaddition is an efficient means to create central, axial, and planar chirality and a variety of chiral organometallic complexes can be used for asymmetric transition-metal-catalyzed inter- and intramolecular reactions. This review summarizes the recent advances in the field of [2+2+2] cycloaddition.1 Introduction2 Formation of Carbocycles2.1 Intermolecular Reactions2.1.1 Cyclotrimerization of Alkynes2.1.2 [2+2+2] Cycloaddition of Two Different Alkynes2.1.3 [2+2+2] Cycloaddition of Alkynes/Alkenes with Alkenes/Enamides2.2 Partially Intramolecular [2+2+2] Cycloaddition Reactions2.2.1 Rhodium-Catalyzed [2+2+2] Cycloaddition2.2.2 Molybdenum-Catalyzed [2+2+2] Cycloaddition2.2.3 Cobalt-Catalyzed [2+2+2] Cycloaddition2.2.4 Ruthenium-Catalyzed [2+2+2] Cycloaddition2.2.5 Other Metal-Catalyzed [2+2+2] Cycloaddition2.3 Totally Intramolecular [2+2+2] Cycloaddition Reactions3 Formation of Heterocycles3.1 Cycloaddition of Alkynes with Nitriles3.2 Cycloaddition of 1,6-Diynes with Cyanamides3.3 Cycloaddition of 1,6-Diynes with Selenocyanates3.4 Cycloaddition of Imines with Allenes or Alkenes3.5 Cycloaddition of (Thio)Cyanates and Isocyanates3.6 Cycloaddition of 1,3,5-Triazines with Allenes3.7 Cycloaddition of Aldehydes with Enynes or Allenes/Alkenes3.8 Totally Intramolecular [2+2+2] Cycloaddition Reactions4 Conclusion

Going Beyond the Carothers, Flory and Stockmayer Equation by Including Cyclization Reactions and Mobility Constraints

A challenge in the field of polymer network synthesis by a step-growth mechanism is the quantification of the relative importance of inter- vs. intramolecular reactions. Here we use a matrix-based kinetic Monte Carlo (kMC) framework to demonstrate that the variation of the chain length distribution and its averages (e.g., number average chain length xn), are largely affected by intramolecular reactions, as mostly ignored in theoretical studies. We showcase that a conventional approach based on equations derived by Carothers, Flory and Stockmayer, assuming constant reactivities and ignoring intramolecular reactions, is very approximate, and the use of asymptotic limits is biased. Intramolecular reactions stretch the functional group (FG) conversion range and reduce the average chain lengths. In the likely case of restricted mobilities due to diffusional limitations because of a viscosity increase during polymerization, a complex xn profile with possible plateau formation may arise. The joint consideration of stoichiometric and non-stoichiometric conditions allows the validation of hypotheses for both the intrinsic and apparent reactivities of inter- and intramolecular reactions. The kMC framework is also utilized for reverse engineering purposes, aiming at the identification of advanced (pseudo-)analytical equations, dimensionless numbers and mechanistic insights. We highlight that assuming average molecules by equally distributing A and B FGs is unsuited, and the number of AB intramolecular combinations is affected by the number of monomer units in the molecules, specifically at high FG conversions. In the absence of mobility constraints, dimensionless numbers can be considered to map the time variation of the fraction of intramolecular reactions, but still, a complex solution results, making a kMC approach overall most elegant.

A novel partitioning scheme for the application of the distortion/interaction - activation strain model to intramolecular reactions

The distortion/interaction or activation strain model, developed by Houk and Bickelhaupt, relates chemical reactivity to the reagents deformations and reciprocal electronic influences. However, in its original formulation, it struggles to elucidate the mechanistic insights of intramolecular reactions, those unimolecular processes in which two parts of a molecule, the reaction centers, linked by a connector, are brought together to yield a different chemical species. Here we present a modification of the distortion/interaction procedure for its application on intramolecular reactions. This new procedure allows the calculation of the influence exerted by the connector over the reaction pathway in an indirect way, from the distortions of the two reaction centers and their interaction energy. This procedure does not include additional, undesired interactions and offers the possibility of calculating very large connectors in a computationally inexpensive way. We applied this methodology in the normal electron-demand Diels–Alder reaction of 1,3,8-nonatriene derivatives, with different functionalizations and connector lengths. In-depth analysis of the IRC showed that the reaction pathway can be subdivided in three main regions, what we called the oncoming, conversion and relaxation phases, each of them characterized by different evolutions of the distortion and interaction energies, and with clear geometry changes. We suggest that this new formulation can provide additional information for intramolecular reactions, especially to those processes for which the connector is said to play a crucial role in the observed reaction rates.

Characterization of Natural and Alkaline-Oxidized Proanthocyanidins in Plant Extracts by Ultrahigh-Resolution UHPLC-MS/MS

In this study, we analyzed the proanthocyanidin (PA) composition of 55 plant extracts before and after alkaline oxidation by ultrahigh-resolution UHPLC-MS/MS. We characterized the natural PA structures in detail and studied the sophisticated changes in the modified PA structures and the typical patterns and models of reactions within different PA classes due to the oxidation. The natural PAs were A- and B-type PCs, PDs and PC/PD mixtures. In addition, we detected galloylated PAs. B-type PCs in different plant extracts were rather stable and showed no or minor modification due to the alkaline oxidation. For some samples, we detected the intramolecular reactions of PCs producing A-type ether linkages. A-type PCs were also rather stable with no or minor modification, but in some plants, the formation of additional ether linkages was detected. PAs containing PD units were more reactive. After alkaline oxidation, these PAs or their oxidation products were no longer detected by MS even though a different type and/or delayed PA hump was still detected by UV at 280 nm. Galloylated PAs were rather stable under alkaline oxidation if they were PC-based, but we detected the intramolecular conversion from B-type to A-type. Galloylated PDs were more reactive and reacted similarly to nongalloylated PDs.

Correlation Between Yield and Reduced Mass of Raw Materials in Enzymatic Reactions

Correlation between the yield in the enzymatic reaction and the molecular weight of the substrate as an approximation of the reduced mass of the raw materials was clarified. The correlation was expressed by the same regression equation as in general organic chemical reactions. The coefficient of the regression equation to distinguish between intramolecular and intermolecular reactions were better when the values for intramolecular reactions were used in the plot of literature yields versus predicted yields. It was also found that the adjustment of the reduced mass by the number of rotatable bonds was not necessary and was found to be a good representation of the characteristics of the enzymatic reaction.

Correlation Between Yield and Reduced Mass of Raw Materials in Enzymatic Reactions

Correlation between the yield in the enzymatic reaction and the molecular weight of the substrate as an approximation of the reduced mass of the raw materials was clarified. The correlation was expressed by the same regression equation as in general organic chemical reactions. The coefficient of the regression equation to distinguish between intramolecular and intermolecular reactions were better when the values for intramolecular reactions were used in the plot of literature yields versus predicted yields. It was also found that the adjustment of the reduced mass by the number of rotatable bonds was not necessary and was found to be a good representation of the characteristics of the enzymatic reaction.

Selectivity between an Alder–ene reaction and a [2 + 2] cycloaddition in the intramolecular reactions of allene-tethered arynes

Substituent-dependent reactivity and selectivity in the intramolecular reactions of arynes tethered with an allene are described.

Catalyst-controlled divergent transformations of N-sulfonyl-1,2,3-triazoles into isoquinolin-3-ones and 2-aminoindanones

A novel catalyst-controlled divergent intramolecular reactions of N-sulfonyl-1,2,3-triazoles with tethered-allylic alcohol has been developed. In the presence of Pd(0) catalyst alone, 1-vinylated 1,4-dihydroisoquinolin-3-ones were formed. Whereas, 3-vinylated 2-aminoindanones were accessed...