Apolysulfide material was synthesized by the direct reaction of sulfur and d-limonene,b y-products of the petroleum and citrus industries,r espectively.T he resulting material was processed into functional coatings or molded into solid devices for the removal of palladium and mercury salts from water and soil. The binding of mercury(II) to the sulfurlimonene polysulfide resulted in acolor change.These properties motivate application in next-generation environmental remediation and mercury sensing.The exploration of sustainable feedstocks is important in the synthesis of functional materials.[1] Herein, we report the utility of apolysulfide synthesized directly from two industrial by-products:s ulfur [2] and d-limonene [3] (Scheme 1). This study was inspired by classic reports on the reaction of sulfur and limonene, [4] theu se of limonene as ar enewable monomer, [5] and the recent and innovative applications of "inverse vulcanization" to access av ariety of advanced materials with high sulfur content. [6] We found that the sulfur-limonene polysulfide can be processed into coatings and solid devices that remove metal salts such as palladium-(II) and mercury(II) from water and soil. We also report the discovery of ac hromogenic response when the polysulfide is exposed to mercury(II). As sulfur is produced annually in excess of 60 million tons as ab y-product of petroleum refining [2] and more than 70 thousand tons of limonene are isolated each year from orange zest in the citrus industry, [3] the sulfur-limonene polysulfide is inexpensive-further motivating its use in metal sequestration, sensing,and environmental remediation.As as tarting point, sulfur was melted (T > 120 8 8C) and then heated to 170 8 8C. Above 150 8 8C, SÀSb ond scission occurs, [7] thereby generating thiyl radicals that could add to limonene.A ne qual mass of limonene was added to the molten sulfur,w hich produced at wo-phase mixture that becomes as ingle,d ark red phase upon reaction. An equal mass of sulfur and limonene was chosen to maximize the content of both industrial by-products in the final material. 1 HNMR analysis of the reaction mixture indicated limonenes exocyclic alkene was consumed more rapidly than its endocyclic alkene,w ith complete consumption of all olefins within 90 min (see Figures S6-S8 in the Supporting Information). Little change was observed by 1 HNMR spectroscopy on further heating. Scheme 1. Synthesis and applicationso fasulfur-limonene polysulfide.