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Copyright of Journal of Sport & Health Research is the property of Journal of Sport & Health Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Sport & Health Research is the property of Journal of Sport & Health Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Sport & Health Research is the property of Journal of Sport & Health Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Sport & Health Research is the property of Journal of Sport & Health Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Sport & Health Research is the property of Journal of Sport & Health Research and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

This work represents a step forward in the understanding of the widely studied photodynamics of alkyl iodides in the first absorption band. Ultraviolet (UV) photodissociation of several alkyl iodides (RI), specifically, a series of linear and ramified molecules with R = C n H 2 n +1 , n = 1-4, at excitation wavelengths of 254 and 268 nm, which correspond to the maximum of the first absorption A-band, has been studied by combining resonance-enhanced multiphoton ionization (REMPI) detection of atomic photofragments I( 2 P 3/2 ) and I*( 2 P 1/2 ) and of pulsed slice imaging. Detailed examination of the total translational energy distributions of both atomic photofragments has been combined with stereodynamical information on the process obtained from the anisotropy β and alignment a 0 2 (∥) and Re[ a 1 2 (∥, ⊥)] parameters to provide a description of the role played by the molecular structure of alkyl iodides in adiabatic and, especially, in nonadiabatic photodissociation dynamics through conical intersections or avoided crossings. The present results suggest that the linear structures couple more efficiently with the pure C-I reaction coordinate, whereas for the branched structures, the coupling with additional vibrational (bending) modes gains importance, showing the dissociation process a multidimensional character. In addition, a large degree of cofragment rotational alignment has been found for the small linear CH 3 I and C 2 H 5 I and, unexpectedly, for the branched t -C 4 H 9 I ( C 3 v symmetry), whereas the rest of the alkyl iodides show low alignment parameters.

Background: Performing an appropriate Class II direct restoration is a great challenge. The correct selection of the matrix system and the elements used for its stabilization will have a great impact on the result. The aim of this study is to show a new digital method for a predictable selection of the wedge and compare it with the conventional method. Methods: Sixty patients were randomly divided into two groups. In Group 0, the wedge was selected intraoperatively by visual examination, while in Group 1 the wedge was selected preoperatively through the measurement of the cervical embrasure on the bite-wing radiography. The number of wedges used, modifications to them, and tissue damage were registered, along with the quality of the proximal contact and the marginal adaptation. Results: Student's t -test revealed a statistical difference between the number of wedges used, which was higher in Group 0 ( p < 0.05). Pearson Chi-square test showed that tissue damage was statistically higher in Group 0 ( p < 0.05), while there was no statistically significant difference between groups in wedge modifications ( p > 0.05). Group 1 revealed a higher frequency of satisfactory proximal contact and marginal adaptation ( p < 0.05). Conclusions: This new technique reduces wedges waste and tissue damage and provides an adequate interproximal anatomy.

The photodissociation dynamics leading to the C-N bond cleavage in methylamine (CH3NH2) are investigated upon photoexcitation in the blue edge of the first absorption A-band, in the 198-204 nm range. Velocity map images of the generated methyl (CH3) fragment detected in specific vibrational modes, i.e., ν = 0, ν1 = 1, and ν2 = 1, through resonance enhanced multiphoton ionization, are presented along with the corresponding translational energy distributions and the angular analysis. The experimental results are complemented by high-level ab initio calculations of potential energy curves as a function of the C-N bond distance. While a similar single Boltzmann-type contribution is observed in all the translational energy distributions measured, the speed-dependent anisotropy parameter obtained through the angular analysis reveals the presence of two different mechanisms. Prompt dissociation through the conical intersection between the Ã1A' first excited state and the ground state located in the exit channel is, indeed, revealed as a minor channel. In contrast, slow dissociation on the ground state, presumably from frustrated N-H bond cleavage trajectories, constitutes the major reaction pathway leading to the methyl formation., (© 2023 Author(s). Published under an exclusive license by AIP Publishing.)

The photodissociation dynamics of methylamine (CH3NH2) upon excitation in the blue edge of the first absorption A-band, in the 198-203 nm range, are investigated by means of nanosecond pump-probe laser pulses and velocity map imaging combined with H(2S)-atom detection through resonance enhanced multiphoton ionization. The images and corresponding translational energy distributions for the H-atoms produced show three different contributions associated with three reaction pathways. The experimental results are complemented by high-level ab initio calculations. The potential energy curves computed as a function of the N-H and C-H bond distances allow us to draw a picture of the different mechanisms. Major dissociation occurs through N-H bond cleavage and it is triggered by an initial geometrical change, i.e., from a pyramidal configuration of the C-NH2 with respect to the N atom to a planar geometry. The molecule is then driven into a conical intersection (CI) seam where three outcomes can take place: first, threshold dissociation into the second dissociation limit, associated with the formation of CH3NH(Ã), is observed; second, direct dissociation after passage through the CI leading to the formation of ground state products; and third, internal conversion into the ground state well in advance to dissociation. While the two last pathways were previously reported at a variety of wavelengths in the 203-240 nm range, the former had not been observed before to the best of our knowledge. The role of the CI and the presence of an exit barrier in the excited state, which modify the dynamics leading the two last mechanisms, are discussed considering the different excitation energies used., (© 2023 Author(s). Published under an exclusive license by AIP Publishing.)

The photodissociation dynamics and photofragment alignment of bromoiodomethane (CH 2 BrI) have been studied at 193 nm using a double experimental and theoretical approach. In addition, the ultraviolet (UV)-vacuum ultraviolet (VUV) absorption spectrum of gas phase CH 2 BrI has been measured in the photon energy range of 5-11 eV using the VUV Fourier transform spectrometer (FTS) at the VUV beamline DESIRS of the synchrotron SOLEIL facility. The slice imaging technique in combination with resonance enhanced multiphoton ionization (REMPI) detection of the Br( 2 P J ) and I( 2 P J ) (with J = 3/2 and 1/2 for Br/I and Br*/I*, respectively) atomic photofragments have been used to produce experimental translational energy and angular distributions, which were analyzed to deliver, on one hand, the partitioning of the available energy among the different degrees-of-freedom of the photofragments and, on the other, the photofragment polarization in terms of a q k ( p ) alignment parameters. The experimental measurements were rationalized in terms of high-level ab initio calculations of vertical excitation energies, transition dipole moments and potential energy curves (PECs) along different reaction coordinates to provide a complete picture of the photodissociation dynamics. The results indicate that for excitation at 193 nm, prompt C-X cleavage (with X being either halogen atom, Br or I) competes with fast internal conversion and consequent stochastic dissociation in lower electronic states. In the case of the CH 2 Br + I( 2 P 3/2 )/I*( 2 P 1/2 ) channels, the dynamics are greatly biased toward the stochastic dissociation process due to both the particular PECs landscape and the unfavored excitation of the CH 2 BrI ensemble with respect to the C-I molecular axis at this excitation energy. The ab initio PECs provide a tentative path for the fast dissociation process in either case. For the C-Br bond breakage, excitation to the 13 A ' electronic state and predissociation through the 11 A '/11 A ″ or 12 A '/12 A ″ states, leading to direct dissociation through the 10 A '/9 A ″ states, appear as the most consistent dynamics. For the C-I channel, predissociation does not become a reliable possibility and a fast internal conversion may precede dissociation through the repulsive 6 A '/6 A ″ and 4 A '/4 A ″ states. The large content of rotational and vibrational excitation of the polyatomic cofragments is justified through the soft impulsive model and the geometrical changes produced along the dissociation pathway. Strikingly, the a q k ( p ) alignment parameters obtained for the Br( 2 P 3/2 ) and I( 2 P 3/2 ) photoproducts indicate that the rotational angular momentum of the CH 2 X (X = I or Br) cofragment appears highly constrained along the recoil direction. Finally, this work presents a highly plausible explanation for the branching ratio of secondary dissociation processes in the photodynamics of CH 2 BrI at 193 nm.

From june 1974 to december 1975, 204 Hancock prosthetic valves were engrafted. The in-hospital mortality was 8.7%. The eight year survival rate was 78.9%. Of the 171 patients who had surgery, 121 reverted to functional class I, 123 had a mild or absent cardiomegaly. After 8 years of follow up 92% of the cases had not thromboembolic episodes. Ninety five percent of the patients with mitral valve replacement and 95% with aortic valve replacement were free of bacterial endocarditis. During the follow-up period; there were 49 valvular malfunctions, 16 of them mild that required no treatment. In 32 cases the alteration was severe and required surgical intervention. Thirty six prosthetic valves had to be removed; 22 of them had degenerative changes, 10 had bacterial endocarditis and in 4 the suture line broke down. After 8 years 77% of the valves were functioning well. The in-hospital mortality after the second valve replacement was 9.4%.