Conformational equilibria, non-bonding interactions and chirality from rotational spectroscopy

The aim of this thesis is to characterize the genuine nature of the non-bonding interactions, such as hydrogen, weak hydrogen and halogen bonding as well as the lone pair•••π interaction, in an environment free from solvent or matrix effects, by using rotational spectroscopy in supersonic expansion. Fluorination and methylation effects, competition between different non-covalent interactions, isomeric preferences are described in the molecular system studied as well as the proton transfer process, the Ubbelohde and the reverse Ubbelohde effects, the internal rotations, and quadrupole couplings which take place. The dissociation energies of the molecular adducts are also estimated and the structural determination of molecules and/or molecular complexes is performed by using isotopologue spectra. Conformational and tautomeric equilibria are investigated for molecules of biological interests, occasionally using the laser ablation technique. Studies have been performed in order to differentiate the enantiomers of chiral molecules, based on opposite phase detection in double quantum coherence experiments

Indagine sulla Teriofauna mediante fototrappolaggio naturalistico nell'ambito dello studio ambientale per l'individuazione delle aree da destinarsi a Parco Comunale nel Comune di Remanzacco (UD)

Mammal camera-trapping survey in the Remanzacco Municipal Park (province of Udine, Italy). The mammals of the Municipal Park of Remanzacco (province of Udine) were surveyed during 2012 and 2013 by means of camera-trapping, together with the opportunistic collection of presence traces and assessing the available literature data. A checklist of the species was compiled for the protected area. The presence of the wildcat, Felis silvestris Schreber, 1777, was also recorded for the first time

A Machine Learning Decision Support System (DSS) for Neuroendocrine Tumor Patients Treated with Somatostatin Analog (SSA) Therapy

The application of machine learning (ML) techniques could facilitate the identification of predictive biomarkers of somatostatin analog (SSA) efficacy in patients with neuroendocrine tumors (NETs). We collected data from 74 patients with a pancreatic or gastrointestinal NET who received SSA as first-line therapy. We developed three classification models to predict whether the patient would experience a progressive disease (PD) after 12 or 18 months based on clinic-pathological factors at the baseline. The dataset included 70 samples and 15 features. We initially developed three classification models with accuracy ranging from 55% to 70%. We then compared ten different ML algorithms. In all but one case, the performance of the Multinomial Naive Bayes algorithm (80%) was the highest. The support vector machine classifier (SVC) had a higher performance for the recall metric of the progression-free outcome (97% vs. 94%). Overall, for the first time, we documented that the factors that mainly influenced progression-free survival (PFS) included age, the number of metastatic sites and the primary site. In addition, the following factors were also isolated as important: adverse events G3-G4, sex, Ki67, metastatic site (liver), functioning NET, the primary site and the stage. In patients with advanced NETs, ML provides a predictive model that could potentially be used to differentiate prognostic groups and to identify patients for whom SSA therapy as a single agent may not be sufficient to achieve a long-lasting PFS

Furanosic forms of sugars: conformational equilibrium of methyl beta-D-ribofuranoside

The investigation of an isolated ribofuranose unit in the gas phase reveals the intrinsic conformational landscape of the biologically active sugar form.We report the rotational spectra of two conformers of methyl b-D-ribofuranoside in a supersonic jet expansion. Both conformers adopt a near twisted (3T2) ring conformation with the methoxy and hydroxymethyl substituents involved in various intramolecular hydrogen bonds.MINECO-FEDER CTQ2015-68148-C2-

Theory Meets Experiment for Noncovalent Complexes: The Puzzling Case of Pnicogen Interactions

A gas-phase nitrogen\u2013nitrogen noncovalent interaction has been unveiled in the nitroethane\u2013trimethylamine complex in an environment free from solvent and matrix effects using rotational spectroscopy in supersonic expansion. Different quantum chemical models (NOCV/CD and NBO) agree in indicating that this interaction largely prevails over the C 12H c5 c5 c5O and C 12H c5 c5 c5N hydrogen bonds. Furthermore, a SAPT analysis shows that electrostatic and dispersion interactions play a comparable role in stabilizing the complex. The conformational landscape exploration and stationary points characterization have been performed using state-of-the-art quantum-chemical computations providing significant insights on structure determination

A butterfly motion of formic acid and cyclobutanone in the 1:1 hydrogen bonded molecular cluster

Producción CientíficaUpon supersonic expansion, formic acid and cyclobutanone (CBU) form a molecular cluster in which the two constituent molecules, linked by OH⋯O and CH⋯O hydrogen bonds, undergo a rapid interconversion between two equivalent forms. The tunneling motion takes place through the rupture and reformation of the C–H⋯O hydrogen bond between the carbonyl oxygen of HCOOH and one of the two hydrogen atoms of the methylenic group adjacent to the cyclobutanone keto group. From the microwave spectra, tunneling energy splittings (ΔE01) have been determined for the parent (1122.756(3) MHz), DCOOH⋯CBU (1084.538(1) MHz) and HCOOD⋯CBU (1180.282(4) MHz) isotopic species. From these splittings, the potential barrier to interconversion has been calculated to be B2 = 39.7(5) cm−1. The tunneling pathway is an asymmetric butterfly-like motion between the two moieties of the adduct, with a barrier at a configuration in which the ring plane of cyclobutanone is coplanar with formic acid.Ministerio de Economía, Industria y Competitividad (CTQ2015- 68148-C2-2-P)Junta de Castilla y León (programa de apoyo a proyectos de investigación – (UNVA-13-3E-2103)Italian MIUR (PRIN project 2010ERFKXL_001

Rich Collection of n-Propylamine and Isopropylamine Conformers: Rotational Fingerprints and State-of-the-Art Quantum Chemical Investigation

The conformational isomerism of isopropylamine and n-propylamine has been investigated by means of an integrated strategy combining high-level quantum-chemical calculations and high-resolution rotational spectroscopy. The equilibrium structures (and thus equilibrium rotational constants) as well as relative energies of all conformers have been computed using the so-called "cheap" composite scheme, which combines the coupled-cluster methodology with second-order Møller-Plesset perturbation theory for extrapolation to the complete basis set. Methods rooted in the density functional theory have been instead employed for computing spectroscopic parameters and for accounting for vibrational effects. Guided by quantum-chemical predictions, the rotational spectra of isopropylamine and n-propylamine have been investigated between 2 and 400 GHz with Fourier transform microwave and frequency-modulation millimeter/submillimeter spectrometers. Spectral assignments confirmed the presence of several conformers with comparable stability and pointed out possible Coriolis resonance effects between some of them

A Journey from Thermally Tunable Synthesis to Spectroscopy of Phenylmethanimine in Gas Phase and Solution

Phenylmethanimine is an aromatic imine with a twofold relevance in chemistry: organic synthesis and astrochemistry. To tackle both aspects, a multidisciplinary strategy has been exploited and a new, easily accessible synthetic approach to generate stable imine-intermediates in the gas phase and in solution has been introduced. The combination of this formation pathway, based on the thermal decomposition of hydrobenzamide, with a state-of-the-art computational characterization of phenylmethanimine laid the foundation for its first laboratory observation by means of rotational electric resonance spectroscopy. Both E and Z isomers have been accurately characterized, thus providing a reliable basis to guide future astronomical observations. A further characterization has been carried out by nuclear magnetic resonance spectroscopy, showing the feasibility of this synthetic approach in solution. The temperature dependence as well as possible mechanisms of the thermolysis process have been examined