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161.
This study explores temporal changes in the dynamics of the Holocene ENSO proxy record of the Laguna Pallcacocha sedimentary data using two entropy quantifiers. In particular, we analyze the possible connections between changes in entropy and epochs of rapid climate change (RCC). Our results indicate that the dynamics of the ENSO proxy record during the RCC interval 9000-8000 BP displays very low entropy (high predictability) that is remarkably different from that of the other RCCs of the Holocene. Both entropy quantifiers point out to the existence of cycles with a period close to 2000 years during the mid-to-late Holocene. Within these cycles, we find a tendency for entropy to increase (predictability to decrease) during the two longer RCC periods (6000-5000 and 3500-2500 BP) which might be associated with the reported increased aridity of the low tropics. 相似文献
162.
A low-temperature gas-phase kinetics study of the reactions and collisional relaxation processes involving C2(X1Sigma(g)+) and C2(a3Pi(u)) in collision with O2 and NO partners at temperatures from 300 to 24 K is reported. The experiments employed a CRESU (Cinétique de Réaction en Ecoulement Supersonique Uniforme) apparatus to attain low temperatures. The C2 species were created using pulsed laser photolysis at 193 nm of mixtures containing C2Cl4 diluted in N2, Ar, or He carrier gas. C2(X1Sigma(g)+) molecules were detected via pulsed laser-induced fluorescence in the (D1Sigma(u)+ <-- X1Sigma(g)+) system, and C2(a3Pi(u)) molecules were detected via pulsed laser-induced fluorescence in the (d 3Pi(g) <-- a 3Pi(u)) system. Relaxation of 3C2 by intersystem crossing induced by oxygen was measured at temperatures below 200 K, and it was found that this process remains very efficient in the temperature range 50-200 K. Reactivity of C2(X1Sigma(g)+) with oxygen became very inefficient below room temperature. Using these two observations, it was found to be possible to obtain the C2(X1Sigma(g)+) state alone at low temperatures by addition of a suitable concentration of O2 and then study its reactivity with NO without any interference coming from the possible relaxation of C2(a3Pi(u)) to C2(X1Sigma(g)+) induced by this reagent. The rate coefficient for reaction of C2(X1Sigma(g)+) with NO was found to be essentially constant over the temperature range 36-300 K with an average value of (1.6 +/- 0.1) x 10(-10) cm3 molecule(-1) s(-1). Reactivity of C2(a3Pi(u)) with NO was found to possess a slight negative temperature dependence over the temperature range 50-300 K, which is in very good agreement with data obtained at higher temperatures. 相似文献
163.
Formation of an organometallic junction by direct bonding of 4-nitrobenzene monolayer on gold surface by diazonium chemistry has been demonstrated by Fourier transform reflection-absorption spectroscopy with s- and p-polarized radiation. 相似文献
164.
Figueroa-Valverde Lauro Diaz Cedillo Francisco Rosas-Nexticapa Marcela Lopez-Ramos Maria Mateu-Armand Virginia Garcimarero-Espino E. Alejandra Ortiz-Ake Yazmin 《Journal of heterocyclic chemistry》2021,58(2):515-522
There are several studies for the synthesis of oxacycle derivatives using some reagents which require special conditions have been reported. The aim of this study was to synthesize two oxocan derivatives from either imidazole or 2-methylimidazole. The chemical structure was evaluated through both 1H NMR and 13C NMR spectroscopic analysis. The results showed a moderate yielding from oxocan derivatives. It should be mentioned that reagents used in this investigation are not expensive and do not require special conditions for handling. 相似文献
165.
Salt‐Induced Adaptation of a Dynamic Combinatorial Library of Pseudopeptidic Macrocycles: Unraveling the Electrostatic Effects in Mixed Aqueous Media 下载免费PDF全文
Joan Atcher Dr. Alejandra Moure Dr. Jordi Bujons Dr. Ignacio Alfonso 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(18):6869-6878
Dynamic combinatorial libraries are powerful systems for studying adaptive behaviors and relationships, as models of more complex molecular networks. With this aim, we set up a chemically diverse dynamic library of pseudopeptidic macrocycles containing amino‐acid side chains with differently charged residues (negative, positive, and neutral). The responsive ability of this complex library upon the increase of the ionic strength has been thoroughly studied. The families of the macrocyclic members concentrating charges of the same sign showed a large increase in its proportion as the ionic strength increases, whereas those with residues of opposite charges showed the reverse behavior. This observation suggested an electrostatic shielding effect of the salt within the library of macrocycles. The top‐down deconvolution of the library allowed us to obtain the fundamental thermodynamic information connecting the library members (exchange equilibrium constants), as well as to parameterize the adaptation to the external stimulus. We also visualized the physicochemical driving forces for the process by structural analysis using NMR spectroscopy and molecular modeling. This knowledge permitted the full understanding of the whole dynamic library and also the de novo design of dynamic chemical systems with tailored co‐adaptive relationships, containing competing or cooperating species. This study highlights the utility of dynamic combinatorial libraries in the emerging field of systems chemistry. 相似文献
166.
Stimuli‐responsive antifouling polyisobutylene‐based biomaterials via modular surface functionalization 下载免费PDF全文
Alejandra Alvarez Albarran Emily Q. Rosenthal‐Kim Jozsef Kantor Lingyun Liu Zhorro Nikolov Judit E. Puskas 《Journal of polymer science. Part A, Polymer chemistry》2017,55(10):1742-1749
This article demonstrates a new, modular approach to surface functionalization that harnesses chain entanglement. A layer of functionalized polyisobutylene, (PIB)‐ω, where ω = ‐OH, ‐thymine (T), ‐hexaethylene glycol (HEG), poly(ethylene glycol) (‐PEG‐OH), methoxy‐functionalized poly(ethylene glycol) (‐PEG‐OCH3), and ‐tetraethylene glycol‐α‐lipoate (TEG‐αL) was adhered to PIB‐based thermoplastic elastomer (TPE) surfaces. X‐ray photoelectron spectroscopy (XPS) at angles ranging from 20° to 75° showed decreasing polar group concentration with increasing penetration depth, confirming segregation of polar groups toward the surface. Water contact angle (WCA) of the PIB‐based TPE dropped from 95° to 79°?83° upon coating, and soaking in water for 24 h further decreased the WCA. Dynamic WCA measurements showed 40–30° receding angles, showing that stimulus from an aqueous environment elicits enrichment of polar groups on the surface. Fibrinogen (Fg) adsorption on the various surfaces was quantified using surface plasmon resonance (SPR). Static and dynamic WCA did not vary significantly among TPE + PIB‐ω surfaces, but there were dramatic differences in Fg adsorption: 256 ng/cm2 was measured on the native TPE, which dropped to 40 and 22 ng/cm2 on PIB‐PEG‐OCH3 and PIB‐PEG‐OH‐coated surfaces. PIB‐TEG‐αL‐coated surfaces presented the lowest Fg adsorption with 14 ng/cm2. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 1742–1749 相似文献
167.
Silva Carlos P. Santander-Nelli Mireya Vera-Oyarce Cristian Silva Juan F. Gómez Alejandra Muñoz Lisa A. Zagal José H. Gulppi Miguel Pavez Jorge 《Journal of Solid State Electrochemistry》2016,20(4):1175-1180
Journal of Solid State Electrochemistry - We report here a novel approach to the template-assisted electrochemical synthesis of vertically aligned polyaniline (PANI) nanostructure surface arrays.... 相似文献
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