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Low humidity detection has always been a challenge in the field of humidity detection. Humidity sensors base on ionic liquid modified metal organic frameworks (MOFs) derived polymer films were prepared in this work. The ionic liquid ligand was uniformly introduced in the frameworks of UIO-66 to enhance the hydrophilicity of sensing materials, the caused defects sites are beneficial for adsorption and desorption, and the MOFs based functional films were easily obtained by in situ photoinduced thiol-ene click reaction. The obtained humidity sensor exhibits a linear response in low relative humidity (RH) range (5% RH - 30% RH) with a tiny humidity hysteresis (~0.2% RH) and short response time to humidity change (response/recovery time is 0.6 s/1.7 s, respectively). ● Humidity sensors based on ionic liquid modified UIO-66 derived polyelectrolyte films were prepared. ● The sensors were prepared facilely in situ on the electrodes by thiol-ene click polymerization in batches. ● The sensor presents linear response under low humidity (5% RH - 30% RH) with a small hysteresis and fast response speed. ● The introduction of ILs and the resulting defect sites are the reasons for effective low humidity detection. [ABSTRACT FROM AUTHOR]

Highlights • Complex 1 is the first long-lived probe to detect IO 4 − in living cells. • Complex 1 has a detection limit of 0.077 μM for IO4− in aqueous buffer, more sensitive than reported fluorescence probes. • The long lifetime of Complex 1 enables its luminescence response to IO4− to be detected in the presence of organic dyes. Abstract Periodate (IO 4 −) is a widely used reagent in organic synthesis and for biomolecular modification. However, highly sensitive fluorescence detection methods for IO 4 − are lacking. In this work, we designed and synthesized iridium(III) complexes for the detection of IO 4 − by the incorporation of a methylthio group to serve as a luminescence trigger. The results showed that complex 1 could detect IO 4 − in a sensitive and selective manner with a detection limit of 0.077 μM, rendering it more sensitive than reported fluorescence methods. Meanwhile, its inherently long emission lifetime enables its luminescence response to IO 4 − to be detected even in the presence of organic dyes by the use of time-resolved emission spectroscopy (TRES). This probe was further demonstrated to detect IO 4 − in living cells. To our knowledge, complex 1 is first long-lived iridium(III)-based probe for the sensitive detection of IO 4 −, and is also one of few existing imaging probes for IO 4 −. [ABSTRACT FROM AUTHOR]

Graphical abstract A pH and thermal stable 3D framework [Mg(ATDC)(H 2 O) 2 ] n (1) as fluorescence sensor with accessible -NH 2 has been successfully synthesized and characterized. It is the first reported highly selective bi-responsive fluorescence Mg-MOF for sensing 2,4,6-Trinitrotoluene(TNT), and have the highest sensitivity for detecting Chromium(III) simultaneously through fluorescence quenching. The quenching mechanisms are mainly attributed to the photo-induced electron transfer and competitive absorptions between the excitation/emission of Mg-MOF and analytes, rather than the interactions between –NH 2 and analytes. Highlights • A new luminescence Mg-MOF was synthesized, the structure was analyzed in detail. • Fluorescent sensing experiment exhibits complex 1 has high sensitivity for 2,4,6-Trinitrotoluene (TNT). • Fluorescent sensing experiment also exhibits complex 1 has high selectivity for Cr3+ ion. • The detection mechanisms and recyclability were studied based on both experiments and calculation. Abstract A pH and thermal stable three dimensional framework [Mg(ATDC)(H 2 O) 2 ] n (1) (H 2 ATDC = 2′-amino-1,1′:4′,1′'-terphenyl-4,4′'-dicarboxylate) with blue fluorescence has been successfully synthesized and characterized. The Mg-MOF contains 2D [Mg(COO) 2 ] n sheet, which links ATDC2− to generate 3D framework with accessible -NH 2 groups, which could be beneficial to impact the reorganization on specific small molecules. Importantly, it is the first reported highly selective fluorescence Mg-MOF for sensing 2,4,6-Trinitrotoluene (TNT), and have the highest sensitivity for detecting Chromium(III) simultaneously through fluorescence quenching. Furthermore, the quenching mechanisms are mainly attributed to the photo-induced electron transfer and competitive absorptions between the excitation/emission of Mg-MOF and analytes, rather than the interactions between –NH 2 and analytes. [ABSTRACT FROM AUTHOR]

[Display omitted] • Humidity sensors based on glycidyl trimethyl ammonium chloride (EPTAC) modified cellulose paper via a facile solution method were fabricated. • The paper is used for the purpose of the humidity sensing material and the sensor substrate. • The as-fabricated paper-based humidity sensor is provided with outstanding humidity sensing properties and good stability. • The humidity sensor was applied to multifunctional applications including human breath rate, non-contact switch and skin humidity. It is of great significance to exploit a simple, cost-effective and environmentally friendly preparation method of multifunctional humidity sensors. However, most humidity sensors need complex manufacturing processes, high cost and narrow usage range. Herein, humidity sensors based on glycidyl trimethyl ammonium chloride (EPTAC) modified cellulose paper via a facile solution method were fabricated, among which the paper is used for the purpose of the humidity sensing material and the sensor substrate. The sensitivity of the obtained sensor was improved by the modification of EPTAC, the response time was decreased to 25 s, which is equivalent to the first-rate paper-based humidity sensors. In addition, the paper-based humidity sensor is provided with well flexibility and biocompatibility, and it exhibits multifunctional applications in respiratory monitoring, non-contact switch and skin humidity monitoring. The low cost and facile preparation technique in this work could provide a useful strategy for developing multifunctional humidity sensor. [ABSTRACT FROM AUTHOR]

Ferroptosis is a form of programmed cell death mostly characterized by a serious misadjustment in the production and degradation of lipid reactive oxygen species (ROS). Meanwhile, numerous studies have indicated that ferroptosis is crucial to the progression and pathophysiology of acute kidney injury (AKI). ROS have been implicated as a pivotal causative factor in cell damage, peroxynitrite (ONOO−) is one of the most prominent ROS which is intimately correlated to ferroptosis-mediated AKI. Therefore, monitoring ONOO− levels in ferroptosis-mediated AKI is important for exploring its physiological and pathological roles. Nevertheless, no probes for detecting ONOO− in ferroptosis-mediated AKI have been reported. Meanwhile, resveratrol (Res) is a bioactive component and has been used to the treatment of AKI. However, the effect of Res on ferroptosis during AKI progression remains elusive. Herein, we evaluated the fluctuation of ONOO− during ferroptosis-mediated AKI using the near-infrared (NIR) fluorescence probe (NFP-ONOO) for the first time. The probe NFP-ONOO showed excellent specificity and sensitivity for the detection of ONOO−. Furthermore, utilizing this probe, we demonstrated Res effectively mitigates AKI induced by folic acid (FA) and cisplatin (CP) by inhibiting ferroptosis. Collectively, this work will provide a powerful guidance for the prophylaxis, diagnosis, and therapy of ferroptosis-mediated AKI. [Display omitted] • A novel near-infrared fluorescent probe NFP-ONOO for ONOO− was fabricated. • The probe NFP-ONOO displayed high selectivity and sensitivity toward ONOO−. • NFP-ONOO was used for imaging ONOO− in cells and zebrafish during ferroptosis. • NFP-ONOO was utilized to image ONOO− in ferroptosis-mediated AKI models. [ABSTRACT FROM AUTHOR]

Self-supported polymer films were fabricated by the thiol-ene click cross-linking reaction in this work. The cross-linked frameworks were used to guarantee the stability the films. The hydrophilic monomer with different contents were introduced into the self-supported thick films and uniformly dispersed in the polymer frameworks. The interdigitated electrodes were screen printed with silver paste on the self-supported films to obtain humidity sensors. Herein, the self-supported film acts as both the sensor substrate and the humidity-sensing material. The humidity sensing performances of the obtained sensors were systematically researched. By optimizing the ratio of hydrophilic monomer in the polymer films, the sensitivities of the sensors were enhanced from 1.58 to 103.75 (in the humidity from 11% RH to 95% RH), the response under low RH environment was significantly improved with good linearity. The response/recovery times of the sensor within the humidity range are measured to be 12.5 s and hundreds of seconds. The prepared flexible sensors possess certain mechanical properties, and exhibit good stability under bending and long-term tests up to 60 days. The applications of the as-prepared sensor in the detection of non-contact human skin humidity, human respiration and relative humidity of green plant were explored. The sensor shows excellent sensing performance in various applications and indicates the potential application in wearable and multifunctional devices. [Display omitted] • Self-supported polymer films were fabricated by the thiol-ene click cross-linking reaction. • Flexible and stable humidity sensors were fabricated by screen printing electrodes on the self-supported films. • The roles of the self-supported film are the substrate of the sensor, as both the humidity-sensing material. • The humidity sensing properties and the multifunctional applications of the obtained sensors were systematically researched. [ABSTRACT FROM AUTHOR]