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Purpose The purpose of this study is to optimize the location of hospitals in Gorgan, Iran, to provide desirable services to citizens in the event of an earthquake crisis. Design/methodology/approach This paper, due to target, is practical and developmental, due to doing method is descriptive and analytical and due to information gathering method is documental and surveying. In the present study, the capabilities of genetic algorithms and imperialist competition algorithm in MATLAB environment in combination with GIS capabilities have been used. In fact, cases such as route blocking, network analysis and vulnerability raster have been obtained from GIS-based on current status data, and then the output of this information is entered as non-random heuristic information into genetic algorithms and imperialist competition algorithm in MATLAB environment. Findings After spatial optimization, the hospital service process has become more favorable. Also, the average cost and transfer vector from hospitals to citizens has decreased significantly. By establishing hospitals in the proposed locations, a larger population of citizens can access relief services in less time. Originality/value Spatial optimization of relief centers, including hospitals, is one of the issues that can be of significant importance, especially in the event of an earthquake crisis. The findings of the present study and the originality, efficiency and innovation of the used methods can provide a favorable theoretical framework for the success of earthquake crisis management projects.

Two-dimensional MoS2 is emerging as a unique platform for a wide range of biomedical applications including extracellular matrix mimics, drug delivery systems and antimicrobial agents. However, low processability and nonspecific interactions at biointerfaces are serious challenges that hamper the biomedical applications of this nanomaterial. Herein, we show how specific interactions between MoS2 and a gelatin matrix results in a biomimetic hydrogel with the self-healing and molecular recognition properties. β-Cyclodextrin was conjugated to the surface of freshly exfoliated MoS2 through a one pot nucleophilic substitution reaction and the obtained cyclodextrin-functionalized MoS2 was used to construct an injectable, self-healable and flexible supramolecular hydrogel upon host-guest interactions with adamantane-modified gelatin matrix. Incorporation of almost 1 wt% of CDMoS2 into gelatin matrix with 1cm2 cross-section resulted in a hydrogel that was able to tolerate one hundred grams. Also, storage modulus (G′), loss modulus (G″) of the obtained hydrogel was 10 and 25 times higher than that for the neat gelatin, respectively. Due to its self-healing, molecular recognition and mechanical properties as well as its flexibility, injectability, and processability, MoS2gel is a promising candidate for a wide range of future biomedical applications including extracellular matrix mimics and tissue engineering.

Today, growing the production of the agricultural sector in order to meet the increasing demand of food is happening through excessive consumption of water resources, energy, chemical fertilizers and pesticides, especially in developing countries. Therefore, the present study aims to design a new approach for sustainable management of resources and realization of clean production in the agricultural sector. In order to design the new approach of the present study, the integration of two concepts of water-energy-food (WEF) nexus and decoupling pollution- agricultural growth (DEC) was used. The proposed approach is modeled through the multi-objective programming model by optimizing the WEF and DEC indices, which is the first research effort in this field. In this regard, the performance of this approach was evaluated in Jiroft county in Kerman province, Iran. The results of the study showed that the consumption of chemical fertilizers and pesticides in the optimal pattern with the simultaneous provision of WEF and gross margin (GM) goals (Optimal 1) is about 110 kg and 0.19 liters per hectare, respectively, more than the proposed pattern (Optimal 3). On the other hand, the consumption of water and energy resources in the optimal pattern with the simultaneous provision of DEC and GM goals (Optimal 2) is about 8785 cubic meters and 1108 MJ per hectare more than the proposed pattern (Optimal 3), respectively. Therefore, this approach, due to the simultaneous integration of two concepts of sustainable development in the agricultural sector, can overcome the weakness of the WEF nexus in not paying attention to the issues of environmental pollution affected by the use of chemical inputs and the weakness of separating pollution- agricultural growth in not paying attention to the management of water and energy resources in the agricultural sector.

Land-use changes are a primary cause of global environmental change. Land use is the management of land cover through human intervention. Study of land-use change in wetlands is largely overlooked as an estimated 30 to 90 % of the world’s wetlands have been destroyed or strongly modified. Therefore, supporting wetland conservation is an urgent priority in three high-level global agendas of 2030. While many factors like global warming and changing climates are key to wetland degradation today, overexploitation by agriculture is the most important destroyer of wetlands in countries like Iran. This study examines the case of the Bakhtegan and Tashak wetland in Iran to determine the factors that influence farmers’ attitudes and behaviors toward wetland conservation. This is done in two phases. The first phase uses remote sensing and GIS to analyze land use changes from 2000 to 2020. The second phase involves surveying farmers to examine the factors behind their intended willingness to participate or support conservation. The data were analyzed using ENVI 5.3, GIS 10.3, SPSS 20, and AMOS 20. The results of phase one reveal a significant increase of bare lands around the wetlands. The survey shows that attitude and subjective norms had positive influences on farmers’ behavioral intentions toward wetland conservation to a statistically significant extent.

Two-dimensional nanomaterials decorated by metal nanoparticles have gained great interest, due to their potential applications in different areas ranging from electrochemical sensing to photothermal therapy. However, metal nanoparticles that are noncovalently immobilized on the surface of two-dimensional nanomaterials can be dissociated from their surface in the complex mediums. This challenge can be overcome by covalent attachment of nanoparticles to the surface of these platforms. In this work, MoS2 sheets are decorated by silver nanoparticles (AgNPs) through a reversible addition-fragmentation chain transfer (RAFT) reaction. Reactive centers were created on the surface of freshly exfoliated MoS2 and a two-dimensional platform with the ability of initiating the RAFT reaction was obtained. Afterwards, silver nanoparticles with acrylamide functionality were synthesized and attached on the surface of MoS2 sheets by the RAFT reaction. MoS2-AgNPs hybrids were characterized by different spectroscopy and microscopy methods as well as thermal and elemental analyses, and then they were used for the electrochemical determination of dipyridamole in aqueous solution. Taking advantage of the straightforward synthesis and the possible MoS2-AgNPs distance adjustment, a variety of hybrid systems with unique physicochemical and optoelectronic properties can be constructed by using this method.

The present study was conducted aiming at the protection of the shallot (Allium altissimum Regal) in natural habitat, which is endangered due to excessive harvesting. In order to increase the sustainability of this product, its wild ecotypes were planted in agricultural land and the effect of bio-fertilizers (nitroxin and phosphate) and sulfur on quantitative (yield and yield components) and qualitative (the active ingredient, allicin, crude protein, and the amount of phosphorus and potassium) traits were investigated. The results showed that the amount of allicin, crude protein, phosphorus, potassium, and yield in the planted ecotypes were significantly higher than the wild type in the studied natural habitat. The results of this study indicated a significant difference respecting quantitative and qualitative trait of cultivated shallot with proper nutritional management compared to wild shallot. Therefore, the expansion and development of this method can lead to the sustainability of the production of shallot and will conserve diversity of its populations in natural habitat.

We thank the German Science Foundation (DFG) for financial support within the grants SFB 765 and SFB 658. M.F.G. and J.P.R. also acknowledge the support of the Cluster of Excellence “Matters of Activity. Image Space Material” funded by the DFG under Germany’s Excellence Strategy EXC 2025-390648296. Furthermore, A.T. acknowledges the DFG for funding within the project TH 1463/12-1. We thank Dr. Andreas Schäfer and Maiko Schulze for solid NMR experiments and we appreciate the effort of Vahid Ahmadi Soureshjani in MALDI-TOF experiments. We acknowledge M. Eng. Jörg M. Stockmann for operating the XPS instrument at the BAM and Prof. Stephanie Reich and Dr. Antonio Setaro for fruitful discussions. 2DTs-HRTEM and -EELS studies were conducted at the Laboratorio de Microscopias Avanzadas, Instituto de Nanociencia de Aragon, Universidad de Zaragoza, Spain. R.A. gratefully acknowledges the support from the Spanish Ministry of Economy and Competitiveness (MINECO) through project grant MAT2016-79776-P (AEI/FEDER, UE) and from the European Union H2020 programs ETN projects “Graphene Flagship” (785219 and 881603), FLAG-ERA - Graphene (MICINN) GATES (PCI2018-093137) and “ESTEEM3” (823717).

While noncovalent interactions at two-dimensional nanobiointerfaces are extensively investigated, less knowledge about covalent interactions at this interface is available. In this work, boronic acid-functionalized 2D MoS2 was synthesized and its covalent multivalent interactions with bacteria and nematodes were investigated. Polymerization of glycidol by freshly exfoliated MoS2 and condensation of 2,5-thiophenediylbisboronic acid on the produced platform resulted in boronic acid-functionalized 2D MoS2. The destructive interactions between 2D MoS2 and bacteria as well as nematodes were significantly amplified by boronic acid functional groups. Because of the high antibacterial and antinematodal activities of boronic acid-functionalized 2D MoS2, its therapeutic efficacy for diabetic wound healing was investigated. The infected diabetic wounds were completely healed 10 days after treatment with boronic acid-functionalized 2D MoS2, and a normal structure for recovered tissues including different layers of skin, collagen, and blood vessels was detected.

While noncovalent interactions between graphene derivatives and biosystems are extensively studied, less knowledge about their covalent multivalent interactions at biointerfaces is available. Due to the affinity of boronic acids towards cis-diol bearing biosystems, graphene sheets with this functionality were synthesized and their covalent interactions with the bacteria and nematode were investigated. As expected, graphene platforms with boronic acid functionality were able to wrap bacteria and destroy it in a short time. Surprisingly, body of nematodes was ruptured and their viability decreased to 30% after 24 h incubation with the functionalized graphene sheets. Because of their antibacterial and antiparasitic activities as well as their ability for wound dressing, graphene platforms with the boronic acid functionality were further investigated for diabetic wound healing. In vivo experiments showed that graphene platforms are more efficient than the commercially available drug, phenytoin, and restore both infected and non-infected diabetic wounds in ten days. Taking advantage of their straightforward synthesis, strong interactions with different biosystems as well as their ability to heal diabetic wounds, the boronic acid functionalized graphene sheets are promising candidates for a broad range of future biomedical applications.

Fluorous biphasic systems use the temperature-sensitive miscibility of fluorinated materials in nonfluorous solutions as a means to control reaction systems and easily separate catalysts or other compounds from a mixture. We present perfluoroalkylated nanographene as a viable platform for photohomogenization and recycling of fluorous-tagged catalysts. The photothermal properties of graphene materials, particularly in the near-infrared range, enable comparatively fast activation time and simplify the recycling of catalysts thanks to the easy separation of the solid fluorinated graphene phase from most solvents by centrifugation. A fluorinated phosphine catalyst was used in a modified, catalyst-regenerative Appel reaction as a model system. The catalyst could be successfully recovered and reused for at least 10 cycles with minimal loss of yield.

Controlled and straightforward functionalization are relevant strategies to obtain MoS2 platforms with defined functionality and improved processability. In this work, an efficient strategy for the functionalization of MoS2 using Reversible Addition Fragmentation Transfer (RAFT) polymerization is reported. The RAFT reagent was directly created on the surface of freshly exfoliated MoS2 and the obtained two-dimensional platform was used for the polymerization of styrene and acrylamide monomers. Various ratios of divinylbenzene were used to crosslink polystyrene brushes and create a polymeric coverage on the surface of MoS2. Furthermore, the polymerization of a mixture of styrene and acrylamide monomers using a MoS2-based RAFT agent resulted in two-dimensional platforms containing copolymer brushes. The structures of the synthesized two-dimensional materials were investigated using different spectroscopy and microscopy techniques as well as thermal and elemental analyses. This research provides an efficient method for the preparation of functional two-dimensional MoS2 nanostructures using RAFT polymerization in gram scale.

Healing of injured tendon is a major clinical challenge in orthopaedic medicine, due to the poor regenerative potential of this tissue. Two-dimensional nanomaterials, as versatile scaffolds, have shown a great potential to support, trigger and accelerate the tendon regeneration. However, weak mechanical properties, poor functionality and low biocompatibility of these scaffolds as well as post-surgery infections are main drawbacks that limit their development in the higher clinical phases. In this work, a series of hydrogels consisting polyglycerol functionalized reduced graphene oxide (PG), polyglycerol-functionalized molybdenum disulfide (PMoS

The attachment of well-defined charge transfer agents to the surface of nanomaterials is an efficient strategy to control their charge density and also to tune their optical, electrical, and physicochemical properties. Particularly interesting are charge transfer agents that either donate or withdraw electrons depending on the arrangements of their building units and that promise a non-destructive attachment to delicate nanomaterials like sp$^2$ compounds. In this work, we rationally synthesize molecular moieties with versatile functionalities. A reactive anchor group allows to attach them to carbon nanotubes as defined charge transfer agents while preserving the tube $\pi$-conjugation. The charge transfer agents were synthesized through the stepwise nucleophilic substitution of either one (monosubstituted series) or two chlorine (disubstituted series) atoms of cyanuric chloride by aniline derivatives containing one, two or three methoxy groups in the para and meta positions. Variation in the number and position of methoxy as an electron transferring group help us to manipulate the electronic and optical properties of the molecular probes and their charge transfer to the SWNTs systematically. The correlation between the optical properties of these molecular probes and their functionality was investigated by experiments and quantum chemical calculations. While the optoelectronic properties of the conjugated charge transfer agents were dominated by the aniline segments, the triazine warrants the ability to nondestructively attach to the surface of SWNTs. This study is one step ahead towards the production of SWNTs with desired optical and electrical properties by covalent $\pi$-preserving functionalization.

Graphene-based hybrid nanomaterials are interestingly being considered in expanding fields such as supercapacitors, biosensors, biomedicine, and pathogen deactivation. Surface properties of the two-dimensional (2D) hybrids are crucial in dictating their safety and efficacy. Therefore, concise and accurate functionalization of the pristine 2D nanomaterials is very important for facilitating their clinical trials. In this case, some of the promising candidates for effective and controllable functionalization of graphene derivatives are dendrimers and hyperbranched polymers because of their high density of tunable functional moieties and their ability to interact with biosystems. Herein, we have reviewed recent advances on designing graphene-dendritic polymer hybrids and their applications together with the challenges in the field.

Recently, many studies have been focused on the development of graphene-based biosensors. However, they rely on one type of signal and need to be calibrated by other techniques. In this study, a nonenzymatic graphene-based biosensor has been designed and constructed. Its ability to detect glucose and Escherichia coli by three different types of signals has been investigated. For its preparation, dopamine-functionalized polyethylene glycol and 2,5-thiophenediylbisboronic acid were conjugated onto the surface of graphene sheets by nitrene [2 + 1] cycloaddition and condensation reactions, respectively. Multivalent interactions between boronic acid segments and biosystems consequently increased the quantifiable fluorescence emission and UV absorption of dopamine segments. Additionally, changing the electrochemical behavior of the functionalized graphene sheets was possible and resulted in a measurable output signal. Conjugation of mannose onto the surface of the biosensor improved its magnitude of signals and specificity for sensing E. coli in a complex medium. The efficiency and accuracy of each signal was monitored by others, which resulted in a real-time self-calibrating biosensor. Taking advantage of the versatility of the three different indicators, including florescence, UV, and electrochemistry, the functionalized graphene sheets have been used as self-regulating biosensors to detect a variety of biosystems with a high accuracy and specificity in a short time.

An understanding of the interactions of 2D nanomaterials with pathogens is of vital importance to developing and controlling their antimicrobial properties. In this work, the interaction of functionalized graphene with tunable hydrophobicity and bacteria is investigated. Poly(ethylene glycol)- block-(poly- N-isopropylacrylamide) copolymer (PEG- b-PNIPAM) with the triazine joint point was attached to the graphene surface by a nitrene [2 + 1] cycloaddition reaction. By thermally switching between hydrophobic and hydrophilic states, functionalized graphene sheets were able to bind to bacteria. Bacteria were eventually disrupted when the functionality was switched to the hydrophobic state. On the basis of measuring the different microscopy methods and a live/dead viability assay, it was found that Escherichia coli ( E. coli) bacteria are more susceptible to hydrophobic interactions than B. cereus bacteria, under the same conditions. Our investigations confirm that hydrophobic interaction is one of the main driving forces at the presented graphene/bacteria interfaces and promotes the antibacterial activity of graphene derivatives significantly.

Interaction of nanoplatforms with biomolecules in biological fluids alters nanoplatforms approach to target tissue and deliver their cargo. Here in, three nanoplatforms were utilized as a carrier to detect the effects of subsequent biomolecules on gene delivery using NIR thermal therapy. Nanoplatforms included; graphene oxide coated gold nanorods (NR@GO), PEGylated NR@GO (NR@GO-PEG) and poly L arginine functionalized NR@GO-PEG (NR@GO-PEG-PLArg). Results indicated that incubation of nanoplatforms in different concentrations of human plasma induced the evolution of layer of proteins (corona) with different thickness on the surface of nanoplatforms. Protein corona decreased the surface charge and optical properties of nanoplatforms. Corona subunits of ITIH, HAS and APOs protein family were extracted from NR@GO-PEG-PLArg surface that play a major role in cellular internalization of nanoplatforms. Moreover, NR@GO-PEG-PLArg remarkably targeted the cancer cells due to uncovered long linear chains of targeting agent (PLArg). The process of gene release and activating apoptotic pathway were enhanced by NIR thermal therapy, which could disrupt the electrostatic interactions and release the protein corona and genes from the surface of nanoplatforms. In conclusion, modification of nanoplatforms with targeting agents could alter the composition of corona toward well interaction with cell and deliver the therapeutic agent.

As resistance to traditional drugs emerges for treatment of virus infections, the need for new methods for virus inhibition increases. Graphene derivatives with large surface areas have shown strong activity against different viruses. However, the inability of current synthetic protocols to accurately manipulate the structure of graphene sheets in order to control their antiviral activity remains a major challenge. In this work, a series of graphene derivatives with defined polyglycerol sulfate and fatty amine functionalities have been synthesized and their interactions with herpes simplex virus type 1 (HSV-1) are investigated. While electrostatic interactions between polyglycerol sulfate and virus particles trigger the binding of graphene to virus, alkyl chains induce a high antiviral activity by secondary hydrophobic interactions. Among graphene sheets with a broad range of alkyl chains, (C3-C18), the C12-functionalized sheets showed the highest antiviral activity, indicating the optimum synergistic effect between electrostatic and hydrophobic interactions, but this derivative was toxic against the Vero cell line. In contrast, sheets functionalized with C6- and C9-alkyl chains showed low toxicity against Vero cells and a synergistic inhibition of HSV-1. This study shows that antiviral agents against HSV-1 can be obtained by controlled and stepwise functionalization of graphene sheets and may be developed into antiviral agents for future biomedical applications.

In this work, a one‐pot approach for the covalent functionalization of few‐layer black phosphorus (BP) by anionic ring opening polymerization of glycidol to obtain multifunctional BP‐polyglycerol (BP‐PG) with high amphiphilicity for near‐infrared‐responsive drug delivery and biocompatibility is reported. Straightforward synthesis in combination with exceptional biological and physicochemical properties designates functionalized BP‐PG as a promising candidate for a broad range of biomedical applications.

Managing the density of charges in carbon nanotubes opens new ways to tune their optical response, their transport properties, and their physico-chemical features. Charge transfer from molecules adsorbed onto the sidewall or filled within the hollow cavity of the nanotubes has already been demonstrated, yet a fine-tunable control of the surface coverage/filling fraction (and thus the amount of transferred charge) remains challenging to achieve. Alternatively, we developed an optically nonperturbing covalent functionalization technique based on the inclusion of a triazine derivative into the carbon network [1]. The nitrogen atom sustaining the attached group becomes an integrated part of the pi-conjugated network and contributes with its lone electron pair to uplifting the position of the Fermi level of the tube. Since the density of attached groups can be varied by adapting the synthetic conditions, this technique offers the advantage of controlling the amount of charge injected into the tubes. Additional groups attached onto the other end of the triazine moiety, moreover, are able to inject charge into the tubes as well. This, for example, allowed us to modulate the photoluminescence of the tubes, switching their emission on and off through the attachment of the switchable spiropyran/merocyanine system [2]. Here we focus on a class of charge-transfer agents that either donate or withdraw electrons depending on the arrangements of their building units [3] and how their decoration affects the properties of the tubes. Figure: Different number of methoxy groups can be attached onto aniline at different positions, resulting in compounds that can either donate or withdraw electrons from the tubes they are attached onto [3]. [1] Setaro et al. Nature Communications 8, 14281 (2017). [2] Godin et al. Science Advances 5, eaax1166 (2019). [3] Fiebor et al. J. Phys. Chem. C. 125, 19925 (2021). Figure 1