@article{pattanayak_mercer_sills_yang_2003, title={Taking stock of agroforestry adoption studies}, volume={57}, DOI={10.1023/a:1024809108210}, journal={Agroforestry Systems}, author={Pattanayak, S. K. and Mercer, D. E. and Sills, Erin and Yang, J. C.}, year={2003}, pages={173–186} }
 @article{martin_yang_dattelbaum_2001, title={Templated synthesis of cuprous chloride networks: Synthesis and characterization of [Hpy]Cu3Cl6 and {[H3NMe](6)Cl}[M3NMe](2)Cu9Cl16}, volume={13}, ISSN={["1520-5002"]}, url={http://www.scopus.com/inward/record.url?eid=2-s2.0-0035090807&partnerID=MN8TOARS}, DOI={10.1021/cm0006648}, abstractNote={Solvothermal reactions with a 1:1 ratio of cuprous chloride and alkylamonium salts as templating agents in acetonitrile or ethanol yield two new polyanionic chains. The trimeric chain [Cu3Cl6]3-, 1, templated by pyridinium cations, crystallizes in the monoclinic space group P21/m with a = 9.1274(8) A, b = 13.2831(5) A, c = 10.0923(7) A, β = 112.562(5)°, and Z = 2. [Cu9Cl16],7- 2, is templated by the complex cation {[H3NMe]6Cl}5+ and two independent [H3NMe]+ cations. The polyanionic chain of 2 is constructed from the condensation of tetrameric cuprous chloride building blocks and crystallizes in the triclinic space group P1 with a = 10.091(2) A, b = 10.173(2) A, c = 23.723(3) A, α = 80.12(1)°, β = 80.99(1)°, γ = 70.68(2)°, and Z = 2. The targeted stoichiometry of [A][CuCl2], with A = pyridinium or methylammonium as templates, results in the formation of condensed oligomeric building blocks that are analogous to those observed for a variety of open-framework group 13 chalcogenides. The relationship between...}, number={2}, journal={CHEMISTRY OF MATERIALS}, author={Martin, JD and Yang, JC and Dattelbaum, AM}, year={2001}, month={Feb}, pages={392–399} }
 @misc{martin_dattelbaum_thornton_sullivan_yang_peachey_1998, title={Metal halide analogues of chalcogenides: A building block approach to the rational synthesis of solid-state materials}, volume={10}, ISSN={["1520-5002"]}, DOI={10.1021/cm9802550}, abstractNote={Principles of solid-state structure and bonding that relate metal-halide and metal-chalcogenide materials are described through a comparison of binary AXn salts. Structural variation is rationalized by a comparison of the size and charge of the respective ions, the d-electron count of the cations, and the type of A−X, A−A, and X−X bonding interactions. These general bonding considerations are exploited for the construction of new metal-halide structure types that are patterned after known chalcogenide structures such as metal-halide analogues of silicates, aluminosilicates, phosphates, and phosphonates.}, number={10}, journal={CHEMISTRY OF MATERIALS}, author={Martin, JD and Dattelbaum, AM and Thornton, TA and Sullivan, RM and Yang, JC and Peachey, MT}, year={1998}, month={Oct}, pages={2699–2713} }