Reactions and reactivity of Co-bpdc coordination polymers (bpdc = 4,4'-biphenyldicarboxylate)

L. Pan, N. Ching, X. Huang, Jing Li

Research output: Contribution to journalArticle

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Abstract

By choosing a suitable metal center, ligand, and solvents, we have revealed several structural transformations involving a polymer precursor, (∞)/1[Co(bpdc)(H2O)2]·H2O (1) was prepared by reaction of Na2bpdc and Co(NO3)2 in aqueous solution. Immersing 1 in pyridine/water solutions of (2:1) and (8:1) ratios yielded a second one-dimensional structure (∞)/1[Co(bpdc)(py)2(H2O)2]·2py (2) and a two-dimensional structure (∞)/2[Co(bpdc)(py)2]·H2O (3), respectively. Afterheating 1 under N2 to remove all water within the structure, the compound Co(bpdc) (I(R)) was obtained. When I(R) was immersed in solutions of pyridine/water (5:4) and in pure pyridine (in air), a third one-dimensional structure of (∞)/1[Co(bpdc)(py)2(H2O)2]·2py·H2O (4) and 3, respectively, were obtained. Compounds 2-4 easily transformed to 1 when immersed in water. Crystal data for 1: monoclinic, space group C2/c with a = 6.950(1), b = 31.585(6), and c = 6.226(1) Å, β = 95.84(3)°, Z = 4. Crystal data for 2: triclinic, space group P1 with a = 9.646(2), b = 10.352(2), and c = 17.031(3) Å, α = 79.02(3)°, β = 86.88(3)°, γ = 77.16(3)°, Z = 2. Crystal data for 3: triclinic, space group P1 with a = 9.137(2), b = 10.480(2), and c = 12.254(2) Å, α = 102.10(3)°, β = 100.80(3)°, γ = 99.43(3)°, Z = 2. Crystal data for 4: orthorhombic, space group Pbcn with a = 13.468(3), b = 16.652 (3), and c = 14.977(3) Å, Z = 4.

Original languageEnglish
Pages (from-to)5333-5340
Number of pages8
JournalInorganic Chemistry
Volume39
Issue number23
DOIs
Publication statusPublished - Nov 13 2000

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coordination polymers
Polymers
reactivity
pyridines
Crystals
Water
water
crystals
Metals
Ligands
aqueous solutions
ligands
air
polymers
Air
metals
pyridine

ASJC Scopus subject areas

  • Inorganic Chemistry

Cite this

Reactions and reactivity of Co-bpdc coordination polymers (bpdc = 4,4'-biphenyldicarboxylate). / Pan, L.; Ching, N.; Huang, X.; Li, Jing.

In: Inorganic Chemistry, Vol. 39, No. 23, 13.11.2000, p. 5333-5340.

Research output: Contribution to journalArticle

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title = "Reactions and reactivity of Co-bpdc coordination polymers (bpdc = 4,4'-biphenyldicarboxylate)",
abstract = "By choosing a suitable metal center, ligand, and solvents, we have revealed several structural transformations involving a polymer precursor, (∞)/1[Co(bpdc)(H2O)2]·H2O (1) was prepared by reaction of Na2bpdc and Co(NO3)2 in aqueous solution. Immersing 1 in pyridine/water solutions of (2:1) and (8:1) ratios yielded a second one-dimensional structure (∞)/1[Co(bpdc)(py)2(H2O)2]·2py (2) and a two-dimensional structure (∞)/2[Co(bpdc)(py)2]·H2O (3), respectively. Afterheating 1 under N2 to remove all water within the structure, the compound Co(bpdc) (I(R)) was obtained. When I(R) was immersed in solutions of pyridine/water (5:4) and in pure pyridine (in air), a third one-dimensional structure of (∞)/1[Co(bpdc)(py)2(H2O)2]·2py·H2O (4) and 3, respectively, were obtained. Compounds 2-4 easily transformed to 1 when immersed in water. Crystal data for 1: monoclinic, space group C2/c with a = 6.950(1), b = 31.585(6), and c = 6.226(1) {\AA}, β = 95.84(3)°, Z = 4. Crystal data for 2: triclinic, space group P1 with a = 9.646(2), b = 10.352(2), and c = 17.031(3) {\AA}, α = 79.02(3)°, β = 86.88(3)°, γ = 77.16(3)°, Z = 2. Crystal data for 3: triclinic, space group P1 with a = 9.137(2), b = 10.480(2), and c = 12.254(2) {\AA}, α = 102.10(3)°, β = 100.80(3)°, γ = 99.43(3)°, Z = 2. Crystal data for 4: orthorhombic, space group Pbcn with a = 13.468(3), b = 16.652 (3), and c = 14.977(3) {\AA}, Z = 4.",
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T1 - Reactions and reactivity of Co-bpdc coordination polymers (bpdc = 4,4'-biphenyldicarboxylate)

AU - Pan, L.

AU - Ching, N.

AU - Huang, X.

AU - Li, Jing

PY - 2000/11/13

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N2 - By choosing a suitable metal center, ligand, and solvents, we have revealed several structural transformations involving a polymer precursor, (∞)/1[Co(bpdc)(H2O)2]·H2O (1) was prepared by reaction of Na2bpdc and Co(NO3)2 in aqueous solution. Immersing 1 in pyridine/water solutions of (2:1) and (8:1) ratios yielded a second one-dimensional structure (∞)/1[Co(bpdc)(py)2(H2O)2]·2py (2) and a two-dimensional structure (∞)/2[Co(bpdc)(py)2]·H2O (3), respectively. Afterheating 1 under N2 to remove all water within the structure, the compound Co(bpdc) (I(R)) was obtained. When I(R) was immersed in solutions of pyridine/water (5:4) and in pure pyridine (in air), a third one-dimensional structure of (∞)/1[Co(bpdc)(py)2(H2O)2]·2py·H2O (4) and 3, respectively, were obtained. Compounds 2-4 easily transformed to 1 when immersed in water. Crystal data for 1: monoclinic, space group C2/c with a = 6.950(1), b = 31.585(6), and c = 6.226(1) Å, β = 95.84(3)°, Z = 4. Crystal data for 2: triclinic, space group P1 with a = 9.646(2), b = 10.352(2), and c = 17.031(3) Å, α = 79.02(3)°, β = 86.88(3)°, γ = 77.16(3)°, Z = 2. Crystal data for 3: triclinic, space group P1 with a = 9.137(2), b = 10.480(2), and c = 12.254(2) Å, α = 102.10(3)°, β = 100.80(3)°, γ = 99.43(3)°, Z = 2. Crystal data for 4: orthorhombic, space group Pbcn with a = 13.468(3), b = 16.652 (3), and c = 14.977(3) Å, Z = 4.

AB - By choosing a suitable metal center, ligand, and solvents, we have revealed several structural transformations involving a polymer precursor, (∞)/1[Co(bpdc)(H2O)2]·H2O (1) was prepared by reaction of Na2bpdc and Co(NO3)2 in aqueous solution. Immersing 1 in pyridine/water solutions of (2:1) and (8:1) ratios yielded a second one-dimensional structure (∞)/1[Co(bpdc)(py)2(H2O)2]·2py (2) and a two-dimensional structure (∞)/2[Co(bpdc)(py)2]·H2O (3), respectively. Afterheating 1 under N2 to remove all water within the structure, the compound Co(bpdc) (I(R)) was obtained. When I(R) was immersed in solutions of pyridine/water (5:4) and in pure pyridine (in air), a third one-dimensional structure of (∞)/1[Co(bpdc)(py)2(H2O)2]·2py·H2O (4) and 3, respectively, were obtained. Compounds 2-4 easily transformed to 1 when immersed in water. Crystal data for 1: monoclinic, space group C2/c with a = 6.950(1), b = 31.585(6), and c = 6.226(1) Å, β = 95.84(3)°, Z = 4. Crystal data for 2: triclinic, space group P1 with a = 9.646(2), b = 10.352(2), and c = 17.031(3) Å, α = 79.02(3)°, β = 86.88(3)°, γ = 77.16(3)°, Z = 2. Crystal data for 3: triclinic, space group P1 with a = 9.137(2), b = 10.480(2), and c = 12.254(2) Å, α = 102.10(3)°, β = 100.80(3)°, γ = 99.43(3)°, Z = 2. Crystal data for 4: orthorhombic, space group Pbcn with a = 13.468(3), b = 16.652 (3), and c = 14.977(3) Å, Z = 4.

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