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- Tartrate-stabilized titanium–oxo clusters containing sulfonate chromophore ligands: synthesis, crystal structures and photochemical properties. Wen-Yu Mou, Bin Xie, Xiao-Long Li, Chuan Lai, Tao Li, Luo Chen, Jian-Shen Feng, Xiao-Xue Bai, Yu Wu, Wei-Ping Wu, Dong-Liang Zhang, Yun-Tian Gu
, New J. Chem.
, 2021
, 45
, 10930
- Synthesis and structural characterization of six Cu(ii)-based coordination polymers using the thermally tunable 1,2,3,4-cyclobutanetetracarboxylic acid. P. Díaz-Gallifa, O. Fabelo, J. Pasán, L. Cañadillas-Delgado, M. A. Ramírez, A. G. Gallardo, C. Ruiz-Pérez
, CrystEngComm
, 2015
, 17
, 5081
- A supramolecular recyclable catalyst for aqueous Suzuki–Miyaura coupling. Miao Qi, Pei Zi Tan, Fei Xue, Haripal Singh Malhi, Zhong-Xing Zhang, David J. Young, T. S. Andy Hor
, RSC Adv.
, 2015
, 5
, 3590
- Synthesis and characterization of organo-scandium and yttrium complexes stabilized by phosphinoamide ligands. Nathan R. Halcovitch, Michael D. Fryzuk
, Dalton Trans.
, 2012
, 41
, 1524
- 57. Exchange studies of certain chelate compounds of the transitional metals. Part VIII. 2,2′,2″-terpyridine complexes. R. Hogg, R. G. Wilkins
, J. Chem. Soc.
, 1962
, 341
- A dicopper (II) complex of a new octaaza macrocycle: a receptor in the entatic state. Sabine Warzeska, Roland Krämer
, Chem. Commun.
, 1996
, 499
- Aryl, methyl-diplatinum complexes each with a metal–metal donor–acceptor bond and bridging 2-diphenylphosphinopyridine (PN) ligands: general synthetic approach and mechanism of isomerization. Bita Shafaatian, Alireza Akbari, S. Masoud Nabavizadeh, Frank W. Heinemann, Mehdi Rashidi
, Dalton Trans.
, 2007
, 4715
- Synthesis and crystal structure of two stereochemical isomers of the trans-dichloro(1,4,8,11-tetraazacyclotetradecane)chromium(III) cation. Luisa M. Flores-Vélez, Javier Sosa-Rivadeneyra, Martha E. Sosa-Torres, María J. Rosales-Hoz, R. A. Toscano
, J. Chem. Soc., Dalton Trans.
, 1991
, 3243
- 598. Phosphonitrilic derivatives. Part X. The crystal structure of trimeric phosphonitrilic fluoride. Maryon W. Dougill
, J. Chem. Soc.
, 1963
, 3211