Hidden Threat: The Influence of Sea-Level Rise on Coastal Groundwater and the Convergence of Impacts on Municipal Infrastructure.

Sea-level rise (SLR) is influencing coastal groundwater by both elevating the water table and shifting salinity profiles landward, making the subsurface increasingly corrosive. Low-lying coastal municipalities worldwide (potentially 1,546, according to preliminary analysis) are vulnerable to an array of impacts spurred by these phenomena, which can occur decades before SLR-induced surface inundation. Damage is accumulating across a variety of infrastructure networks that extend partially and fully beneath the ground surface. Because the resulting damage is largely concealed and imperceptible, it is largely overlooked as part of infrastructure management and planning. Here, we provide an overview of SLR-influenced coastal groundwater and related processes that have the potential to damage societally critical infrastructure and mobilize urban contamination. In an effort to promote research efforts that can inform effective adaptation and management, we discuss various impacts to critical infrastructure and propose actions based on literature focused specifically on SLR-influenced coastal groundwater.

9-Triptycenecarboxylate-Bridged Diiron(II) Complexes: Capture of the Paddlewheel Geometric Isomer.

The synthesis and characterization of diiron(II) complexes supported by 9-triptycenecarboxylate ligands ((-)O(2)CTrp) is described. The interlocking nature of the triptycenecarboxylates facilitates formation of quadruply bridged diiron(II) complexes of the type [Fe(2)(µ-O(2)CTrp)(4)(L)(2)] (L = THF, pyridine or imidazole derivative) with a paddlewheel geometry. A systematic lengthening of the Fe-Fe distance occurs with the increase in steric bulk of the neutral donor L, resulting in values of up to 3 Å without disassembly of the paddlewheel structure. Reactions with an excess of water do not lead to decomposition of the diiron(II) core, indicating that these quadruply bridged complexes are of exceptional stability. The red-colored complexes [Fe(2)(µ-O(2)CTrp)(4)(4-AcPy)(2)] (10) and [Fe(2)(µ-O(2)CTrp)(4)(4-CNPy)(2)] (11) exhibit solvent-dependent thermochromism in coordinating solvents that was studied by variable temperature UV-vis spectroscopy. Reaction of [Fe(2)(µ-O(2)CTrp)(4)(THF)(2)] with N,N,N',N'-tetramethylethylenediamine (TMEDA), tetra-n-butyl ammonium thiocyanate, or excess 2-methylimidazole resulted in the formation of mononuclear complexes [Fe(O(2)CTrp)(2)(TMEDA)] (13), (n-Bu(4)N)(2)[Fe(O(2)CTrp)(2)(SCN)(2)] (14), and [Fe(O(2)CTrp)(2)(2-MeIm)(2)] (15) having an O(4)/N(2) coordination sphere composition.