Humanistic and Holistic Strategies for Combating Mental Health Sequelae in the Elderly During the Post-COVID Era.

Background: The elderly population is rapidly growing worldwide. By the year 2050, the elderly population will increase up to 2.1 billion.

Structure-Spectroscopy Correlation in the Self-Assembled Perylene Diimide-Based Dimers via Inter-Chromophore Coupling.

The impact of conformational change on the ground and excited states of seven perylene diimide (PDI)-based dimeric systems is examined by introducing longitudinal shift, transverse shift, and rotation of one monomer with respect to another. The minimum energy conformations are compared via an energy decomposition analysis. The heteroatom-substituted dimeric systems, such as B N-embedded PDI, trans-thio-PDI (trans-S-PDI), and N-PDI, show BN···π, C═S···π, and N···H interactions that survive over a longer range of longitudinal and transverse shifts.

CRISPR/Cas9 opens new horizon of crop improvement under stress condition.

Plants are exposed to a myriad of stresses, stemming from abiotic and biotic sources, significantly threatening agricultural productivity. The low crop yield, coupled with the global burden of population has resulted in the scarcity of quality food, exacerbating socio-economic issues like poverty, hunger, and malnutrition. Conventional breeding methods for the generation of stress-tolerant plants are time-consuming, limit genetic diversity, and are not sustainable for the consistent production of high-yielding crops.

Design, Synthesis, and Characterization of Organometallic BODIPY-Ru(II) Dyads: Redox and Photophysical Properties with Singlet Oxygen Generation Capability†.

A series of Ru(II)-acetylide complexes (, , and ) with alkynyl-functionalized borondipyrromethene (BODIPY) conjugates were designed by varying the position of the linker that connects the BODIPY unit to the Ru(II) metal center through acetylide linkage at either the 2-() and 2,6-() or the -phenyl () position of the BODIPY scaffold. The Ru(II) organometallic complexes were characterized by various spectroscopic methods, including nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, CHN, and high-resolution mass spectrometry (HRMS) analyses. The Ru(II)-BODIPY conjugates exhibit fascinating electrochemical and photophysical properties.

A sequential Friedländer and anionic benzannulation strategy for the regiodefined assembly of unsymmetrical acridines.

An efficient sequential double-annulation strategy has been developed to afford a series of unsymmetrical acridines with high yield and regioselectivity for the first time. This simple protocol enables the sequential assembly of two aromatic rings from simple starting materials. The reaction proceeds modified Friedländer annulation and subsequent base-mediated benzannulation with acrylates as Michael acceptors.

Combined effect of yoga and naturopathy in uncomplicated varicose vein disease - a prospective randomized controlled trial.

Background: Though the treatment of uncomplicated varicose vein (UVV) might prevent late complications such as skin change or ulceration, but, there are limited studies available to justify this concept. Yoga and Naturopathy being a proficient tool in managing non communicable diseases including many cardiovascular diseases; no attempt was made to study its potential effect in Varicose Vein diseases.

Objective: The present study aims to study the combination of Yoga and Naturopathy in uncomplicated varicose vein patients.

Self-Assembling Behaviour of Perylene, Perylene Diimide, and Thionated Perylene Diimide Deciphered through Non-Covalent Interactions.

The π-conjugated supramolecular polymers (SMP) have gained vast popularity in materials chemistry and biomedicine due to their spectacular self-assembling behaviour. A detailed account of the electronic structure and bonding through quantum theory of atoms-in-molecules, non-covalent interactions, and energy decomposition analysis (EDA) in the oligomers of perylene, perylene diimide (PDI), and thionated-PDI (t-PDI) is presented. The oligomers of all three molecules show a slip angle of θ≈62° thus forming H-aggregates.

SARS-CoV-2 Infections, Impaired Tissue, and Metabolic Health: Pathophysiology and Potential Therapeutics.

The SARS-CoV-2 enters the human airways and comes into contact with the mucous membranes lining the mouth, nose, and eyes. The virus enters the healthy cells and uses cell machinery to make several copies itself. Critically ill patients infected with SARS-CoV-2 may have damaged lungs, air sacs, lining, and walls.

Mitochondrial Modulations, Autophagy Pathways Shifts in Viral Infections: Consequences of COVID-19.

Mitochondria are vital intracellular organelles that play an important role in regulating various intracellular events such as metabolism, bioenergetics, cell death (apoptosis), and innate immune signaling. Mitochondrial fission, fusion, and membrane potential play a central role in maintaining mitochondrial dynamics and the overall shape of mitochondria. Viruses change the dynamics of the mitochondria by altering the mitochondrial processes/functions, such as autophagy, mitophagy, and enzymes involved in metabolism.

Management of acute calculus cholecystitis with integrated Ayurveda and Yoga intervention: A case report.

Acute calculus cholecystitis (ACC) is a frequently reported medical condition in general practice. Approximately 20% of patients with gallbladder stones experience ACC in their lifetime. Ayurveda and Yoga are ancient traditional systems of medicine used for treatment of diseases and improving and maintaining health.

Efficacy of Integrated Yoga and Ayurveda Rasayana on cognitive functions in elderly with mild cognitive impairment: Non-randomized three-arm clinical trial.

Background: Yoga and Ayurveda are ancient sciences which emphasize on the cure of disease and the proportion of health. Both sciences are also known to reduce the aging process and are helpful in aging-related disorders.

Objective: This study investigates the effects of Yoga and Ayurveda Rasayana combined intervention on cognition among the elderly with mild cognitive impairment.

Impact of Yoga on cognition and mental health among elderly: A systematic review.

Background: Cognitive decline and psychological health problems are the most frequently observed and under-treated issues among the elderly. Many studies have assessed the efficacy of Yoga on cognitive and mental health parameters among the elderly. However, up to date, there is no systematic review done to evaluate the role of Yoga-based interventions on cognition and mental health in the elderly.

Role of Substituents at 3-position of Thienylethynyl Spacer on Electronic Properties in Diruthenium(II) Organometallic Wire-like Complexes.

A series of organometallic complexes [Cl(dppe) Ru-C≡C-(3-R-C H S)-C≡C-Ru(dppe) Cl] (3-R-C H S=3-substituted thienyl moiety; R=-H, -C H , -C H , -C H , -C H , -OMe, -CN in 5 a-5 g respectively) have been synthesized by systematic variation of 3-substituents at the thienylethynyl bridging unit. The diruthenum(II) wire-like complexes (5 a-5 g) have been achieved by the reaction of thienylethynyl bridging units, HC≡C-(3-R-C H S)-C≡CH (4 a-4 g) with cis-[Ru(dppe) Cl ]. The wire-like diruthenium(II) complexes undergo two consecutive electrochemical oxidation processes in the potential range of 0.

A water-soluble BODIPY based 'OFF/ON' fluorescent probe for the detection of Cd ions with high selectivity and sensitivity.

A water-soluble dilithium salt BODIPY derivative (LiBDP) with appended dicarboxylate pseudo-crown ether [NO4] coordinating sites has been designed, synthesized and characterized successfully for the selective and sensitive recognition of Cd2+ in aqueous media. The chemosensor exhibits a remarkable increase in fluorescence intensity as well as a distinct color change upon the addition of Cd2+ over other environmentally and biologically relevant metal ions in H2O. The fluorometric response of LiBDP is attributed to the metal chelation-enhanced fluorescence (MCHEF) effect which has been confirmed by a strong association constant of 2.

Synthesis, Structure, Electrochemical, and Spectroscopic Properties of Hetero-Bimetallic Ru(II)/Fe(II)-Alkynyl Organometallic Complexes.

A series of heterobimetallic wire-like organometallic complexes [( tpy-CH-R)(PPh)Ru-C≡C-Fc] ( tpy-CH-R = 4'-(aryl)-2,2':6',2''-terpyridyl, Fc = [(η-Cp)Fe], R = -H, -Me, -F, -NMe in complexes 5-8, respectively) featuring ferrocenyl and 4'-(aryl)-2,2':6',2''-terpyridyl ruthenium(II) complexes as redox active metal termini, have been synthesized. Various spectroscopic tools, such as multinuclear NMR, IR spectra, HRMS, CHN analyses, and single crystal X-ray crystallography have been utilized to characterize the heterobimetallic complexes. The electrochemical and UV-vis-NIR spectroscopic studies have been investigated to evaluate the electronic delocalization across the molecular backbones of the Ru(II)-Fe(II) heterobinuclear organometallic dyads.

Synthesis, structure, and photophysical and electrochemical properties of Ru(ii) complexes of arylene-vinylene terpyridyl conjugates.

A series of arylene-vinylene π-conjugated terpyridyl ruthenium(ii) complexes, [Ru(PPh3)2Cl(tpy-C6H4-CH[double bond, length as m-dash]CH-Ar)][PF6] (1-4; tpy = 2,2':6',2''-terpyridyl, where Ar = phenyl, tolyl, 1-naphthyl and 9-anthracenyl as substituents at the 4' position of tpy), have been synthesized and characterized by multinuclear NMR, IR, HRMS and single crystal X-ray crystallography. The influence of the electronic nature of arylene groups on their photophysical and electrochemical properties has been investigated to understand the electronic interaction between the metal-organic redox centers. Furthermore, a σ-donor phenylacetylide group has been incorporated to accomplish [Ph-C[triple bond, length as m-dash]C-Ru(PPh3)2(tpy-C6H4-CH[double bond, length as m-dash]CH-Ar)][PF6] (5-8) complexes by the substitution of a coordinated chloride ligand and to investigate the change in their redox and photophysical properties.

Diruthenium(ii)-capped oligothienylethynyl bridged highly soluble organometallic wires exhibiting long-range electronic coupling.

Organometallic molecular wires with π-conjugation along their molecular backbones are of considerable interest for application in molecular-scale electronics. In this regard, thienylethynyl-based π-conjugated oligomers of three, five and seven thienylethynyl units with -C[triple bond, length as m-dash]C-H termini have been successfully synthesized through stepwise Pd(0)/Cu(i)-catalyzed Sonogashira coupling. The corresponding highly soluble diruthenium(ii) diacetylide complexes (O1-Ru2, O3-Ru2, O5-Ru2 and O7-Ru2, respectively) have been prepared by the reaction of cis-Ru(dppe)2Cl2 and NaPF6 in DCM with the corresponding rigid rod-like thienylethynyl oligomers with one, three, five and seven thienylethynyl π-conjugated segments containing alkynyl termini (O1, O3, O5 and O7).

Investigation of Yoga Pranayama and Vedic Mathematics on Mindfulness, Aggression and Emotion Regulation.

Background: Competitive examinations, particularly in mathematics, have made emotional stress a major problem for preuniversity students, emotions like aggression toward fellow students and teachers increase. Mindfulness is a quality that reduces both emotional stress and aggression, so increasing mindfulness should be helpful.

Aims: To study the effects of Yoga Pranayama (YP) and Vedic Mathematics (VM) on mindfulness, aggression, and emotion regulation.

A Mild Rhodium Catalyzed Direct Synthesis of Quinolones from Pyridones: Application in the Detection of Nitroaromatics.

A rhodium catalyzed direct regioselective oxidative annulation by double C-H activation is described to synthesize highly substituted quinolones from pyridones. The reaction proceeds at mild conditions with broad scope and wide functional group tolerance. These novel quinolones were explored to recognize nitroaromatic compounds.

Achieving yellow emission by varying the donor/acceptor units in rod-shaped fluorenyl-alkynyl based π-conjugated oligomers and their binuclear gold(i) alkynyl complexes.

Fluorenyl-alkynyl based π-conjugated rod-shaped oligomers bearing different central aromatic moieties and functionalizable di-alkynyl termini, such as H-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-H (OH1), H-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Btz-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-H (OH2) and H-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Btd-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-H (OH3) where Fl = 9,9-dioctylfluorene, Btz = N-hexylbenzotriazole, and Btd = benzothiadiazole, were successfully synthesized by a Pd(0) catalyzed Stille coupling protocol. Electron withdrawing benzothiadiazole and benzotriazole as strong to moderate acceptors and fluorene as the donor have been incorporated to adjust the Donor-Acceptor (D-A) strength for fine-tuning the bandgap (E) as well as the emission wavelength. The corresponding digold(i) σ-complexes (PPh)Au-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Au(PPh) (OM1), (PPh)Au-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Btz-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Au(PPh) (OM2) and (PPh)Au-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Btd-[triple bond, length as m-dash]-Fl-[triple bond, length as m-dash]-Au(PPh) (OM3) have also been prepared by a reaction of Au(PPh)Cl and methanolic NaOMe in DCM with the corresponding alkynyl functionalized oligomers to take advantage of the heavy-atom effect on their emissive properties.

Dimensional control of block copolymer nanofibers with a π-conjugated core: crystallization-driven solution self-assembly of amphiphilic poly(3-hexylthiophene)-b-poly(2-vinylpyridine).

With the aim of accessing colloidally stable, fiberlike, π-conjugated nanostructures of controlled length, we have studied the solution self-assembly of two asymmetric crystalline-coil, regioregular poly(3-hexylthiophene)-b-poly(2-vinylpyridine) (P3HT-b-P2VP) diblock copolymers, P3HT23-b-P2VP115 (block ratio=1:5) and P3HT44-b-P2VP115 (block ratio=ca. 1:3). The self-assembly studies were performed under a variety of solvent conditions that were selective for the P2VP block.

Tetragonal and helical morphologies from polyferrocenylsilane block polyelectrolytes via ionic self-assembly.

The use of ionic self-assembly, a facile non-covalent approach, to access non-conventional block copolymer morphologies, including tetragonal and helical structures, from a combination of polyferrocenylsilane diblock copolymer polyelectrolytes and AOT-based surfactants, is described.

Responsive vesicles from the self-assembly of crystalline-coil polyferrocenylsilane-block-poly(ethylene oxide) star-block copolymers.

We demonstrate the synthesis and characterization of star-shaped crystalline-coil block copolymers with four arms consisting of an inner block of poly(ethylene oxide) and an outer semicrystalline compartment of poly(ferrocenyldimethylsilane), [PEO(50) -b-PFDMS(35)](4). The materials were synthesized by transition-metal-catalyzed ring-opening polymerization of dimethylsila[1]ferrocenophane in the presence of silane-functionalized four-arm PEO stars as macroinitiators and they exhibited a moderate polydispersity (PDI≅1.4).

The coordination and polymerisation of cyclic 1,3-dienes by gold(I) cations.

Cyclopentadiene and 1,3-cyclohexadiene are readily polymerised by [LAu][X]. With specific ancillary ligands polymerisation was suppressed and a molecular species involving an Au(I) cation η(2)-bonding CpH was isolated and whose structure was probed in both the solid state and in solution.