TY - JOUR
T1 - Modification of Network and Pore Dimensionality in Metal-Organic Frameworks Containing a Secondary Phosphine Functionality
AU - Bezrukov, Andrey A.
AU - Törnroos, Karl W.
AU - Dietzel, Pascal D.C.
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/6/7
Y1 - 2017/6/7
N2 - Three new metal-organic frameworks containing a triphenylphosphine moiety, namely, [Zn3(tpp)2(DMF)2]·nDMF (1), [Zn3(tpp)2(4,4′-bpy)2]·nDMF (2), and [Zn3(tpp)2(3,3′-bpy)]·nDMF (3), were synthesized using 4,4′,4″-phosphanetriyltribenzoic acid (H3tpp) as a tritopic linker. The absence or presence of additional N-donor linker molecules in the reaction mixture lead to the formation of (3,6)-c layered, (3,8)-c pillared layered, or (3,4,6)-c frameworks. Compound 1 is composed of a trinuclear zinc secondary building unit (SBU) and the tpp3- anion arranged in a layered (3,6)-c network with kgd topology. There are DMF guest molecules coordinated to the terminal Zn atoms of the trinuclear inorganic SBU. The addition of the neutral N-donor molecules 3,3′-bipyridine (3,3′-bpy) and 4,4′-bipyridine (4,4′-bpy) as second organic linker molecule lead to an increase of dimensionality of the networks. Compound 2 is a (3,4,6)-nodal three-dimensional MOF. Its structure consists of two equivalent interpenetrated nets with the point symbol (52·64)(52·6)2(54·66·72·8·92) containing solvent filled pockets. The free electron pair of the phosphorus atom of the triphenylphosphine moiety is pointing toward the zero-dimensional pores. The structure of 3 can be described as layers of 1 which are connected by 3,3′-bipyridine as pillar into a three-dimensional (3,8)-c network with the point symbol (43)2(46·618·84). The non-interpenetrated structure of 3 contains a solvent filled three-dimensional pore system. All three materials exhibit uptake of CO2 at 195 K after removal of the guest DMF molecules. This is particularly surprising for 2, with its zero-dimensional pores in the single-crystal structure and absence of N2 adsorption at 77 K. Compound 3 shows a large gate opening effect for CO2 adsorption at 195 K.
AB - Three new metal-organic frameworks containing a triphenylphosphine moiety, namely, [Zn3(tpp)2(DMF)2]·nDMF (1), [Zn3(tpp)2(4,4′-bpy)2]·nDMF (2), and [Zn3(tpp)2(3,3′-bpy)]·nDMF (3), were synthesized using 4,4′,4″-phosphanetriyltribenzoic acid (H3tpp) as a tritopic linker. The absence or presence of additional N-donor linker molecules in the reaction mixture lead to the formation of (3,6)-c layered, (3,8)-c pillared layered, or (3,4,6)-c frameworks. Compound 1 is composed of a trinuclear zinc secondary building unit (SBU) and the tpp3- anion arranged in a layered (3,6)-c network with kgd topology. There are DMF guest molecules coordinated to the terminal Zn atoms of the trinuclear inorganic SBU. The addition of the neutral N-donor molecules 3,3′-bipyridine (3,3′-bpy) and 4,4′-bipyridine (4,4′-bpy) as second organic linker molecule lead to an increase of dimensionality of the networks. Compound 2 is a (3,4,6)-nodal three-dimensional MOF. Its structure consists of two equivalent interpenetrated nets with the point symbol (52·64)(52·6)2(54·66·72·8·92) containing solvent filled pockets. The free electron pair of the phosphorus atom of the triphenylphosphine moiety is pointing toward the zero-dimensional pores. The structure of 3 can be described as layers of 1 which are connected by 3,3′-bipyridine as pillar into a three-dimensional (3,8)-c network with the point symbol (43)2(46·618·84). The non-interpenetrated structure of 3 contains a solvent filled three-dimensional pore system. All three materials exhibit uptake of CO2 at 195 K after removal of the guest DMF molecules. This is particularly surprising for 2, with its zero-dimensional pores in the single-crystal structure and absence of N2 adsorption at 77 K. Compound 3 shows a large gate opening effect for CO2 adsorption at 195 K.
UR - http://www.scopus.com/inward/record.url?scp=85020276896&partnerID=8YFLogxK
U2 - 10.1021/acs.cgd.7b00243
DO - 10.1021/acs.cgd.7b00243
M3 - Article
AN - SCOPUS:85020276896
SN - 1528-7483
VL - 17
SP - 3257
EP - 3266
JO - Crystal Growth and Design
JF - Crystal Growth and Design
IS - 6
ER -