Who benefits from the "sharing" economy of Airbnb?

Sharing economy platforms have become extremely popular in the last few years, and they have changed the way in which we commute, travel, and borrow among many other activities. Despite their popularity among consumers, such companies are poorly regulated. For example, Airbnb, one of the most successful examples of sharing economy platform, is often criticized by regulators and policy makers. While, in theory, municipalities should regulate the emergence of Airbnb through evidence-based policy making, in practice, they engage in a false dichotomy: some municipalities allow the business without imposing any regulation, while others ban it altogether. That is because there is no evidence upon which to draft policies. Here we propose to gather evidence from the Web. After crawling Airbnb data for the entire city of London, we find out where and when Airbnb listings are offered and, by matching such listing information with census and hotel data, we determine the socio-economic conditions of the areas that actually benefit from the hospitality platform. The reality is more nuanced than one would expect, and it has changed over the years. Airbnb demand and offering have changed over time, and traditional regulations have not been able to respond to those changes. That is why, finally, we rely on our data analysis to envision regulations that are responsive to real-time demands, contributing to the emerging idea of “algorithmic regulation”

Three Cationic: Nonporous CuI-Coordination Polymers: Structural Investigation and Vapor Iodine Capture

Three cationic nonporous copper(I) coordination polymers containing bis-pyrazolyl flexible ligands have been prepared and characterized, namely, [Cu(\u3bc-bdb)1.5](PF6)n (1), [Cu(\u3bc-bpb)2](PF6)n (2), and [Cu(\u3bc-bpmb)2](PF6)n (3) (bdb = 1,4-bis(3,5-dimethylpyrazolyl) methyl)benzene; bpb = 1,4-bis(pyrazolyl)butane; bpmb = 1,4-bis(pyrazolyl)methyl)benzene). All compounds were characterized by infrared, powder X-ray diffraction, elemental and thermal analyses, and single-crystal X-ray diffraction. Compound 1, with methyl-substituted pyrazolyl ligand, forms a chain of alternating rings and ribbons in which the copper(I) centers are three coordinated in distorted trigonal planar geometry. In compounds 2 and 3 copper(I) atoms adopt distorted tetrahedral geometries giving two-dimensional sheet structures with 44-sql topology. Interestingly, iodine sorption experiments show that colorless crystals of 2 and 3 remain unchanged in the presence of iodine vapors, while the three-coordinated compound 1 immediately absorbs iodine and turns dark. Anion exchange behavior of compounds 1 and 2 was also investigated both in solution and in the solid state

Influence of the counter anion and steric hindrance of pyrazolyl and imidazolyl flexible ligands on the structure of zinc-based coordination polymers

Treatments of flexible 1,4-bis(3,5-dimethylpyrazolyl)butane (bbd), 1,4-bis(imidazolyl)butane (bib) and 1,4-bis(2-methylimidazolyl)butane (bmib) ligands with zinc salts at room temperature, resulted in the formation of four novel metal\u2013organic coordination architectures: [ZnI2(l-bbd)]n (1), [Zn(NCS)2(l-bbd)]n (2), {[Zn(l-bib)2](ClO4)2 (Et2O)0.5 (H2O)0.25}n (3) and {[Zn(l-bmib)2](ClO4)2 (H2O)4}n (4). X-ray crystallographic analyses show different 1D and 3D polymeric structures for compounds 1\u20134 due to the variation of the counter anions, solvent, steric hindrance and position of donating atoms in the structure of flexible ligands. In 1 and 2, one-dimensional (1D) zig-zag polymeric chains are formed via metal centers and l-bbd ligands. Complex 3 shows a 3-fold interpenetrated 3D architecture with 10^3-ths network topology. In contrast to 3, in the structure of 4 neighboring Zn(II) ions are interconnected by a double-bridging l-bmib ligands to form an infinite 1D polymeric double chain. The conformations of the flexible ligands were analyzed in detail

Entangled Two-Dimensional Coordination Networks: A General Survey

Many of the reported species exhibit the intriguing feature of interpenetration or other types of entanglements. The properties of these materials are related not only to their molecular structures but also to the topology of the individual networks as well as to the way in which the individual nets are entangled. Different synthetic procedures have been developed to attain a certain control of entanglement in coordination networks, and recently some reviews have appeared that are focused on factors governing the entanglements, having in mind their potential applications. However, these analyses are mostly devoted to 3D networks thanks to the great wealth of data on interpenetration. Simplification of a network that contains 2-loops can lead to complete disappearance of the entanglement, and therefore such networks were picked out into a separate group

Diorganotin(IV) complexes with 2-furancarboxylic acid hydrazone derivative of benzoylacetone : synthesis, X-ray structure, antibacterial activity, DNA cleavage and molecular docking

Two new diorganotin(IV) complexes, Me2SnL and Ph2SnL, have been synthesized from the reaction of Me2SnCl2 and Ph2SnCl2 with the hydrazone H2L [H2L \ubc (Furan-2-yl) (5-hydroxy-3-methyl-5-phenyl-4,5- dihydro-1H-pyrazol-1-yl)-methanone] derived from furan-2-carbohydrazide and benzoylacetone. The new compounds have been characterized by elemental and spectroscopic analyses. The crystal structures of the monohydrate form of the ligand and of the Me2SnL derivative have been also determined by X-ray crystallography. Experimental evidences confirm the existence of the hydrazone ligand exclusively in cyclic form in both solution and solid state. On coordination to tin the hydrazone undergoes a ring opening reaction and a doubly deprotonation to act as a tridentate ligand via imine nitrogen and enolic oxygens. The tin atom in the complexes is five coordinate with geometry between square-pyramidal and trigonal-bipyramidal. The in vitro antibacterial activity of ligand and its complexes has been evaluated against Gram-positive (Bacillus subtilis and Staphylococcus aureus) and Gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacteria. The interaction between compounds with bacterial DNA was also studied by molecular docking. Our findings indicate that diphenyltin(IV) complex, by binding to DNA via minor groove to TATA sequence in genes upstream, has good activities along with the standard antibacterial drugs. Our agarose-gel electrophoresis experiments show that the ligand exert DNA cleavage, while Me2SnL and Ph2SnL did not

Sleep-related epileptic behaviors and non-REM-related parasomnias: Insights from stereo-EEG

During the last decade, many clinical and pathophysiological aspects of sleep-related epileptic and non-epileptic paroxysmal behaviors have been clarified. Advances have been achieved in part through the use of intracerebral recording methods such as stereo-electroencephalography (S-EEG), which has allowed a unique "in vivo" neurophysiological insight into focal epilepsy. Using S-EEG, the local features of physiological and pathological EEG activity in different cortical and subcortical structures have been better defined during the entire sleep-wake spectrum. For example, S-EEG has contributed to clarify the semiology of sleep-related seizures as well as highlight the specific epileptogenic networks involved during ictal activity. Moreover, intracerebral EEG recordings derived from patients with epilepsy have been valuable to study sleep physiology and specific sleep disorders. The occasional co-occurrence of NREM-related parasomnias in epileptic patients undergoing S-EEG investigation has permitted the recordings of such events, highlighting the presence of local electrophysiological dissociated states and clarifying the underlying pathophysiological substrate of such NREM sleep disorders. Based on these recent advances, the authors review and summarize the current and relevant S-EEG literature on sleep-related hypermotor epilepsies and NREM-related parasomnias. Finally, novel data and future research hypothesis will be discussed

Diversifying molecular and topological space via a supramolecular solid-state synthesis: a purely organic mok net sustained by hydrogen bonds

A three-dimensional hydrogen-bonded network based on a rare mok topology has been constructed using an organic molecule synthesized in the solid state. The molecule is obtained using a supramolecular protecting-group strategy that is applied to a solid-state [2+2] photodimerization. The photodimerization affords a novel head-to-head cyclobutane product. The cyclobutane possesses tetrahedrally disposed cis-hydrogen-bond donor (phenolic) and cis-hydrogen- bond acceptor (pyridyl) groups. The product self-assembles in the solid state to form a mok network that exhibits twofold interpenetration. The cyclobutane adopts different conformations to provide combinations of hydrogen-bond donor and acceptor sites to conform to the structural requirements of the mok net

Self-assembly of three cationic silver(I) coordination networks with flexible bis(pyrazolyl)-based linkers

Three new cationic silver(I) coordination polymers, {[Ag(mu-bpmb)](SO3CF3)}n (1), {[Ag(mu-bdb)1.5] (SO3CF3)}n (2) and {[Ag(mu-bpb)2](NO3)}n (3), with flexible 1,4-bis[(pyrazolyl)methyl]benzene (bpmb), 1,4-bis[(3,5-dimethylpyrazolyl)methyl]benzene (bdb), and 1,4-bis(pyrazolyl)butane (bpb) have been prepared at room temperature by the solvent layering method. The three compounds were characterized by FT-IR spectroscopy, PXRD, elemental analyses and single-crystal X-ray diffraction. Compound 1 is a highly undulated polymeric 1D chain in which the silver ions adopt a linear geometry, coordinating two bpmb linkers. Compounds 2 and 3 are both 2D coordination polymers with their silver atoms being three and four coordinated, and resulting in 6^3-hcb and 4^4-sql underlying net topologies, respectively. The flexible bispyrazolyl ligands display various conformations in the solid state, causing the formation of different Ag. . .Ag separations in the polymeric structures