1) Aya, Toshihiro; Hamilton, Andrew D. Bioorg. & Med. Chem. Lett. 2003, 13(16), 2651-2654 DOI:10.1016/S0960-894X(03)00551-1 ;Tetrabiphenylporphyrin-based receptors for protein surfaces show sub-nanomolar affinity and enhance unfolding
2) Q. Lin , X. Bu , A. Kong , C. Mao , X. Zhao , F. Bu and P. Feng , J. Am. Chem. Soc., 2015, 137 , 2235-2238, DOI:10.1021/jacs.5b00076 ; New Heterometallic Zirconium Metalloporphyrin Frameworks and Their Heteroatom-Activated High-Surface-Area Carbon Derivatives
3) T. C. Wang , W. Bury , D. A. Gómez-Gualdrón , N. A. Vermeulen , J. E. Mondloch , P. Deria , K. Zhang , P. Z. Moghadam , A. A. Sarjeant , R. Q. Snurr , J. F. Stoddart , J. T. Hupp and O. K. Farha , J. Am. Chem. Soc., 2015, 137 , 3585-3591, DOI: 10.1021/ja512973b ; Ultrahigh Surface Area Zirconium MOFs and Insights into the Applicability of the BET Theory
4) J. Zheng, M. Wu, F. Jiang, W. Su, M. Hong, Chem. Sci., 2015,6, 3466-3470, DOI: 10.1039/C5SC00213C ; Stable porphyrin Zr and Hf metal–organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses