Subjects judged verbally on temporal order between pressing a switch and a marking sound (MS) in a simple reaction time paradigm. They were uncertain when sound preceded movement by less than about 60 ms or followed it by less than 130 ms (transient zone--TZ). The point of subjective equality (defined by 0.5 probability of correct judgements of temporal order of sound and switching onsets) and the median of TZ were shifted about 60 and 35 ms prior movement onset, respectively. Estimating mutual timing of movement preparation and execution and sensory delays, these shifts correspond to the simultaneity of onsets of MS and proprioceptive feedback in the brain. Thus the results suggest about proprioceptive origin of perception of active movement onset.
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http://dx.doi.org/10.1097/00001756-199206000-00018 | DOI Listing |
Acc Chem Res
January 2025
Organisch-Chemisches Institut, Universität Münster, Corrensstrasse 40, 48149 Münster, Germany.
ConspectusSkeletal editing, which involves adding, deleting, or substituting single or multiple atoms within ring systems, has emerged as a transformative approach in modern synthetic chemistry. This innovative strategy addresses the ever-present demand for developing new drugs and advanced materials by enabling precise modifications of molecular frameworks without disrupting essential functional complexities. Ideally performed at late stages of synthesis, skeletal editing minimizes the need for the cost- and labor-intensive processes often associated with synthesis, thus accelerating the discovery and optimization of complex molecular architectures.
View Article and Find Full Text PDFLangmuir
January 2025
Materials Chemistry Department, CSIR-Institute of Minerals and Materials Technology, Bhubaneswar, Odisha 751013, India.
Due to the high cost of the available Pt electrocatalysts, the large-scale water electrolysis production of hydrogen has been hindered. Hydrogen generation via electrochemical water splitting is a renewable energy essential to a sustainable society, creating a distinct material interface that shows Pt-like properties with long-term stability crucial to hydrogen evolution reactions (HERs). Here, we synthesized the guanine-assisted facile synthesis of 1 wt % Pt/MoC/C having a layered type morphology via solid state calcined process followed by chemical reduction.
View Article and Find Full Text PDFLangmuir
January 2025
Department of Chemical Engineering, Canakkale Onsekiz Mart University,17100 Canakkale, Turkey.
Radioactive iodine, a key waste product of nuclear energy, has been a significant concern among nuclear materials because of its high volatility and its ability to easily enter the human metabolism. Porous materials containing a large number of N-heterocyclic units such as carbazole in the skeletons use as effective adsorbents showing high iodine capture capacities. Herein, a new carbazole-bismaleimide-based hyper-cross-linked porous organic polymer (CzBMI-POP) was successfully prepared from a new tetra-armed carbazole-maleimide monomer (Bis-Cz(BMI)), which contains biscarbazole units and maleimide side groups.
View Article and Find Full Text PDFJ Chem Inf Model
January 2025
Theoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
In the field of computational chemistry, predicting bond dissociation energies (BDEs) presents well-known challenges, particularly due to the multireference character of reactive systems. Many chemical reactions involve configurations where single-reference methods fall short, as the electronic structure can significantly change during bond breaking. As generating training data for partially broken bonds is a challenging task, even state-of-the-art reactive machine learning interatomic potentials (MLIPs) often fail to predict reliable BDEs and smooth dissociation curves.
View Article and Find Full Text PDFInorg Chem
January 2025
Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Science, 630090 Novosibirsk, Russia.
The photoinduced reaction of [Pt(NO)] with pyridine or its derivatives (L) was found to result in the formation of [PtL](NO) salts in high yield. This transformation was successfully probed for methyl- and carboxyethyl-substituted pyridines, and the corresponding [PtL](NO) salts were isolated and fully characterized using single-crystal X-ray diffraction (SCXRD). Anation of the [Pt(py)] cationic complex with N was studied by H NMR spectroscopy in aqueous and water/dimethyl sulfoxide solutions of [Pt(py)](NO).
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